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dbSNP Short Genetic Variations

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs731236

Current Build 153

Released July 9, 2019

Organism
Homo sapiens
Position
chr12:47844974 (GRCh38.p12) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.32714 (82106/250982, GnomAD_exome)
G=0.32372 (40649/125568, TOPMED)
G=0.33385 (40509/121340, ExAC) (+ 9 more)
G=0.2635 (20725/78642, PAGE_STUDY)
G=0.3308 (10313/31172, GnomAD)
G=0.3554 (4622/13006, GO-ESP)
G=0.277 (1385/5008, 1000G)
G=0.354 (1587/4480, Estonian)
G=0.400 (1543/3854, ALSPAC)
G=0.405 (1500/3708, TWINSUK)
G=0.06 (34/610, Vietnamese)
G=0.41 (243/600, NorthernSweden)
Clinical Significance
Reported in ClinVar
Gene : Consequence
VDR : Synonymous Variant
Publications
309 citations
Genomic View
See rs on genome
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p12 chr 12 NC_000012.12:g.47844974A>G
GRCh37.p13 chr 12 NC_000012.11:g.48238757A>G
VDR RefSeqGene NG_008731.1:g.65058T>C
Gene: VDR, vitamin D receptor (minus strand)
Molecule type Change Amino acid[Codon] SO Term
VDR transcript variant 2 NM_001017535.1:c.1056T>C I [ATT] > I [ATC] Coding Sequence Variant
vitamin D3 receptor isoform VDRA NP_001017535.1:p.Ile352= I (Ile) > I (Ile) Synonymous Variant
VDR transcript variant 1 NM_001364085.1:c.1056T>C I [ATT] > I [ATC] Coding Sequence Variant
vitamin D3 receptor isoform VDRAx NP_001351014.1:p.Ile352= I (Ile) > I (Ile) Synonymous Variant
VDR transcript variant 1 NM_000376.3:c.1056T>C I [ATT] > I [ATC] Coding Sequence Variant
vitamin D3 receptor isoform VDRA NP_000367.1:p.Ile352= I (Ile) > I (Ile) Synonymous Variant
VDR transcript variant 3 NM_001017536.2:c.1206T>C I [ATT] > I [ATC] Coding Sequence Variant
vitamin D3 receptor isoform VDRB1 NP_001017536.1:p.Ile402= I (Ile) > I (Ile) Synonymous Variant
VDR transcript variant X2 XM_011538720.2:c.1056T>C I [ATT] > I [ATC] Coding Sequence Variant
vitamin D3 receptor isoform X2 XP_011537022.1:p.Ile352= I (Ile) > I (Ile) Synonymous Variant
VDR transcript variant X3 XM_006719587.3:c.1056T>C I [ATT] > I [ATC] Coding Sequence Variant
vitamin D3 receptor isoform X2 XP_006719650.1:p.Ile352= I (Ile) > I (Ile) Synonymous Variant
VDR transcript variant X1 XM_024449178.1:c.1125T>C I [ATT] > I [ATC] Coding Sequence Variant
vitamin D3 receptor isoform X1 XP_024304946.1:p.Ile375= I (Ile) > I (Ile) Synonymous Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Allele: G (allele ID: 331082 )
ClinVar Accession Disease Names Clinical Significance
RCV000361773.1 Vitamin D-Dependent Rickets Likely-Benign
RCV000616832.1 not specified Benign
Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
gnomAD - Exomes Global Study-wide 250982 A=0.67286 G=0.32714
gnomAD - Exomes European Sub 134976 A=0.60967 G=0.39033
gnomAD - Exomes Asian Sub 48984 A=0.7598 G=0.2402
gnomAD - Exomes American Sub 34570 A=0.7874 G=0.2126
gnomAD - Exomes African Sub 16256 A=0.7242 G=0.2758
gnomAD - Exomes Ashkenazi Jewish Sub 10062 A=0.6406 G=0.3594
gnomAD - Exomes Other Sub 6134 A=0.640 G=0.360
TopMed Global Study-wide 125568 A=0.67628 G=0.32372
ExAC Global Study-wide 121340 A=0.66615 G=0.33385
ExAC Europe Sub 73310 A=0.6078 G=0.3922
ExAC Asian Sub 25148 A=0.7521 G=0.2479
ExAC American Sub 11572 A=0.8003 G=0.1997
ExAC African Sub 10402 A=0.7206 G=0.2794
ExAC Other Sub 908 A=0.67 G=0.33
The PAGE Study Global Study-wide 78642 A=0.7365 G=0.2635
The PAGE Study AfricanAmerican Sub 32488 A=0.7140 G=0.2860
The PAGE Study Mexican Sub 10792 A=0.7680 G=0.2320
The PAGE Study Asian Sub 8318 A=0.894 G=0.106
The PAGE Study PuertoRican Sub 7916 A=0.670 G=0.330
The PAGE Study NativeHawaiian Sub 4530 A=0.801 G=0.199
The PAGE Study Cuban Sub 4230 A=0.641 G=0.359
The PAGE Study Dominican Sub 3826 A=0.676 G=0.324
The PAGE Study CentralAmerican Sub 2448 A=0.751 G=0.249
The PAGE Study SouthAmerican Sub 1980 A=0.759 G=0.241
The PAGE Study NativeAmerican Sub 1260 A=0.675 G=0.325
The PAGE Study SouthAsian Sub 854 A=0.68 G=0.32
gnomAD - Genomes Global Study-wide 31172 A=0.6692 G=0.3308
gnomAD - Genomes European Sub 18772 A=0.6255 G=0.3745
gnomAD - Genomes African Sub 8632 A=0.712 G=0.288
gnomAD - Genomes East Asian Sub 1554 A=0.954 G=0.046
gnomAD - Genomes Other Sub 1086 A=0.652 G=0.348
gnomAD - Genomes American Sub 838 A=0.73 G=0.27
gnomAD - Genomes Ashkenazi Jewish Sub 290 A=0.59 G=0.41
GO Exome Sequencing Project Global Study-wide 13006 A=0.6446 G=0.3554
GO Exome Sequencing Project European American Sub 8600 A=0.606 G=0.394
GO Exome Sequencing Project African American Sub 4406 A=0.721 G=0.279
1000Genomes Global Study-wide 5008 A=0.723 G=0.277
1000Genomes African Sub 1322 A=0.715 G=0.285
1000Genomes East Asian Sub 1008 A=0.933 G=0.067
1000Genomes Europe Sub 1006 A=0.600 G=0.400
1000Genomes South Asian Sub 978 A=0.63 G=0.37
1000Genomes American Sub 694 A=0.74 G=0.26
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.646 G=0.354
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.600 G=0.400
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.595 G=0.405
A Vietnamese Genetic Variation Database Global Study-wide 610 A=0.94 G=0.06
Northern Sweden ACPOP Study-wide 600 A=0.59 G=0.41
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement A= G Note
GRCh38.p12 chr 12 NC_000012.12:g.47844974= NC_000012.12:g.47844974A>G
GRCh37.p13 chr 12 NC_000012.11:g.48238757= NC_000012.11:g.48238757A>G
VDR RefSeqGene NG_008731.1:g.65058= NG_008731.1:g.65058T>C
VDR transcript variant 1 NM_000376.3:c.1056= NM_000376.3:c.1056T>C
VDR transcript variant 1 NM_000376.2:c.1056= NM_000376.2:c.1056T>C
VDR transcript variant 3 NM_001017536.2:c.1206= NM_001017536.2:c.1206T>C
VDR transcript variant 3 NM_001017536.1:c.1206= NM_001017536.1:c.1206T>C
VDR transcript variant 2 NM_001017535.1:c.1056= NM_001017535.1:c.1056T>C
VDR transcript variant 1 NM_001364085.1:c.1056= NM_001364085.1:c.1056T>C
VDR transcript variant X3 XM_006719587.3:c.1056= XM_006719587.3:c.1056T>C
VDR transcript variant X2 XM_011538720.2:c.1056= XM_011538720.2:c.1056T>C
VDR transcript variant X1 XM_024449178.1:c.1125= XM_024449178.1:c.1125T>C
vitamin D3 receptor isoform VDRA NP_000367.1:p.Ile352= NP_000367.1:p.Ile352=
vitamin D3 receptor isoform VDRB1 NP_001017536.1:p.Ile402= NP_001017536.1:p.Ile402=
vitamin D3 receptor isoform VDRA NP_001017535.1:p.Ile352= NP_001017535.1:p.Ile352=
vitamin D3 receptor isoform VDRAx NP_001351014.1:p.Ile352= NP_001351014.1:p.Ile352=
vitamin D3 receptor isoform X2 XP_006719650.1:p.Ile352= XP_006719650.1:p.Ile352=
vitamin D3 receptor isoform X2 XP_011537022.1:p.Ile352= XP_011537022.1:p.Ile352=
vitamin D3 receptor isoform X1 XP_024304946.1:p.Ile375= XP_024304946.1:p.Ile375=
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

113 SubSNP, 12 Frequency, 2 ClinVar submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss76497 Oct 05, 2000 (86)
2 HGBASE ss2420961 Nov 14, 2000 (89)
3 SNP500CANCER ss5586953 Jul 02, 2003 (116)
4 WI_SSAHASNP ss12216651 Jul 11, 2003 (116)
5 CUORCGL ss12568608 Aug 26, 2003 (117)
6 SC_SNP ss14739713 Dec 05, 2003 (119)
7 EGP_SNPS ss16359245 Feb 27, 2004 (120)
8 JDRF_WT_DIL ss20420895 Apr 05, 2004 (121)
9 PERLEGEN ss24395756 Sep 20, 2004 (123)
10 ERASMUSMC-GLIM ss32465678 Dec 02, 2004 (126)
11 ABI ss38908577 Mar 11, 2006 (126)
12 ILLUMINA ss65743935 Oct 16, 2006 (127)
13 EILEEN ss68316101 Dec 12, 2006 (127)
14 ILLUMINA ss74882784 Dec 06, 2007 (129)
15 KRIBB_YJKIM ss80755731 Dec 15, 2007 (130)
16 CORNELL ss86241970 Mar 23, 2008 (129)
17 CANCER-GENOME ss86343777 Mar 23, 2008 (129)
18 BCMHGSC_JDW ss89137833 Mar 24, 2008 (129)
19 KRIBB_YJKIM ss119365123 Dec 01, 2009 (131)
20 ENSEMBL ss133153445 Dec 01, 2009 (131)
21 SEATTLESEQ ss159726127 Dec 01, 2009 (131)
22 ILLUMINA ss160871589 Dec 01, 2009 (131)
23 ILLUMINA ss174334971 Jul 04, 2010 (132)
24 COMPLETE_GENOMICS ss175117861 Jul 04, 2010 (132)
25 BUSHMAN ss198140414 Jul 04, 2010 (132)
26 BCM-HGSC-SUB ss208325743 Jul 04, 2010 (132)
27 1000GENOMES ss210817036 Jul 14, 2010 (132)
28 1000GENOMES ss211279905 Jul 14, 2010 (132)
29 1000GENOMES ss225741831 Jul 14, 2010 (132)
30 1000GENOMES ss235926865 Jul 15, 2010 (132)
31 1000GENOMES ss242488033 Jul 15, 2010 (132)
32 ILLUMINA ss244309162 Jul 04, 2010 (132)
33 GMI ss286557561 Apr 25, 2013 (138)
34 NHLBI-ESP ss342354324 May 09, 2011 (134)
35 PAGE_STUDY ss469996522 May 04, 2012 (137)
36 ILLUMINA ss481541541 May 04, 2012 (137)
37 ILLUMINA ss481570547 May 04, 2012 (137)
38 ILLUMINA ss482543948 Sep 08, 2015 (146)
39 ILLUMINA ss485565762 May 04, 2012 (137)
40 1000GENOMES ss491040673 May 04, 2012 (137)
41 CLINSEQ_SNP ss491663924 May 04, 2012 (137)
42 ILLUMINA ss537462688 Sep 08, 2015 (146)
43 TISHKOFF ss563151808 Apr 25, 2013 (138)
44 SSMP ss658704745 Apr 25, 2013 (138)
45 ILLUMINA ss778600539 Sep 08, 2015 (146)
46 ILLUMINA ss783228428 Sep 08, 2015 (146)
47 ILLUMINA ss784182648 Sep 08, 2015 (146)
48 ILLUMINA ss832488800 Sep 08, 2015 (146)
49 ILLUMINA ss834057824 Sep 08, 2015 (146)
50 JMKIDD_LAB ss974483343 Aug 21, 2014 (142)
51 EVA-GONL ss989508319 Aug 21, 2014 (142)
52 JMKIDD_LAB ss1067533218 Aug 21, 2014 (142)
53 JMKIDD_LAB ss1078444304 Aug 21, 2014 (142)
54 1000GENOMES ss1344913977 Aug 21, 2014 (142)
55 HAMMER_LAB ss1397633434 Sep 08, 2015 (146)
56 DDI ss1426926728 Apr 01, 2015 (144)
57 EVA_GENOME_DK ss1576268438 Apr 01, 2015 (144)
58 EVA_FINRISK ss1584081433 Apr 01, 2015 (144)
59 EVA_DECODE ss1599178741 Apr 01, 2015 (144)
60 EVA_UK10K_ALSPAC ss1628540160 Apr 01, 2015 (144)
61 EVA_UK10K_TWINSUK ss1671534193 Apr 01, 2015 (144)
62 EVA_EXAC ss1690872933 Apr 01, 2015 (144)
63 EVA_MGP ss1711328072 Apr 01, 2015 (144)
64 EVA_SVP ss1713325787 Apr 01, 2015 (144)
65 ILLUMINA ss1752069124 Sep 08, 2015 (146)
66 HAMMER_LAB ss1807234224 Sep 08, 2015 (146)
67 WEILL_CORNELL_DGM ss1932872881 Feb 12, 2016 (147)
68 ILLUMINA ss1959431957 Feb 12, 2016 (147)
69 JJLAB ss2027187806 Sep 14, 2016 (149)
70 ILLUMINA ss2094793385 Dec 20, 2016 (150)
71 ILLUMINA ss2095034753 Dec 20, 2016 (150)
72 USC_VALOUEV ss2155523374 Dec 20, 2016 (150)
73 HUMAN_LONGEVITY ss2189575466 Dec 20, 2016 (150)
74 TOPMED ss2353507935 Dec 20, 2016 (150)
75 SYSTEMSBIOZJU ss2628073749 Nov 08, 2017 (151)
76 ILLUMINA ss2632956191 Nov 08, 2017 (151)
77 GRF ss2699866169 Nov 08, 2017 (151)
78 GNOMAD ss2739762403 Nov 08, 2017 (151)
79 GNOMAD ss2748852328 Nov 08, 2017 (151)
80 GNOMAD ss2910200516 Nov 08, 2017 (151)
81 AFFY ss2984973696 Nov 08, 2017 (151)
82 AFFY ss2985615942 Nov 08, 2017 (151)
83 SWEGEN ss3009644027 Nov 08, 2017 (151)
84 ILLUMINA ss3021427636 Nov 08, 2017 (151)
85 EVA_SAMSUNG_MC ss3023067748 Nov 08, 2017 (151)
86 BIOINF_KMB_FNS_UNIBA ss3027402142 Nov 08, 2017 (151)
87 TOPMED ss3170201336 Nov 08, 2017 (151)
88 CSHL ss3350053056 Nov 08, 2017 (151)
89 ILLUMINA ss3625622658 Oct 12, 2018 (152)
90 ILLUMINA ss3626870894 Oct 12, 2018 (152)
91 ILLUMINA ss3630965562 Oct 12, 2018 (152)
92 ILLUMINA ss3633019492 Oct 12, 2018 (152)
93 ILLUMINA ss3633720378 Oct 12, 2018 (152)
94 ILLUMINA ss3634502637 Oct 12, 2018 (152)
95 ILLUMINA ss3635411171 Oct 12, 2018 (152)
96 ILLUMINA ss3636188350 Oct 12, 2018 (152)
97 ILLUMINA ss3637162153 Oct 12, 2018 (152)
98 ILLUMINA ss3637961234 Oct 12, 2018 (152)
99 ILLUMINA ss3640209970 Oct 12, 2018 (152)
100 ILLUMINA ss3642954991 Oct 12, 2018 (152)
101 OMUKHERJEE_ADBS ss3646441402 Oct 12, 2018 (152)
102 ILLUMINA ss3651804106 Oct 12, 2018 (152)
103 ILLUMINA ss3651804107 Oct 12, 2018 (152)
104 ILLUMINA ss3653746832 Oct 12, 2018 (152)
105 EGCUT_WGS ss3676920453 Jul 13, 2019 (153)
106 EVA_DECODE ss3693619605 Jul 13, 2019 (153)
107 ILLUMINA ss3725322219 Jul 13, 2019 (153)
108 ACPOP ss3738999867 Jul 13, 2019 (153)
109 ILLUMINA ss3744803327 Jul 13, 2019 (153)
110 EVA ss3750449665 Jul 13, 2019 (153)
111 PAGE_CC ss3771688748 Jul 13, 2019 (153)
112 ILLUMINA ss3772302817 Jul 13, 2019 (153)
113 KHV_HUMAN_GENOMES ss3815780035 Jul 13, 2019 (153)
114 1000Genomes NC_000012.11 - 48238757 Oct 12, 2018 (152)
115 The Avon Longitudinal Study of Parents and Children NC_000012.11 - 48238757 Oct 12, 2018 (152)
116 Genetic variation in the Estonian population NC_000012.11 - 48238757 Oct 12, 2018 (152)
117 ExAC NC_000012.11 - 48238757 Oct 12, 2018 (152)
118 gnomAD - Genomes NC_000012.11 - 48238757 Jul 13, 2019 (153)
119 gnomAD - Exomes NC_000012.11 - 48238757 Jul 13, 2019 (153)
120 GO Exome Sequencing Project NC_000012.11 - 48238757 Oct 12, 2018 (152)
121 Northern Sweden NC_000012.11 - 48238757 Jul 13, 2019 (153)
122 The PAGE Study NC_000012.12 - 47844974 Jul 13, 2019 (153)
123 TopMed NC_000012.12 - 47844974 Oct 12, 2018 (152)
124 UK 10K study - Twins NC_000012.11 - 48238757 Oct 12, 2018 (152)
125 A Vietnamese Genetic Variation Database NC_000012.11 - 48238757 Jul 13, 2019 (153)
126 ClinVar RCV000361773.1 Oct 12, 2018 (152)
127 ClinVar RCV000616832.1 Oct 12, 2018 (152)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID History Updated (Build)
rs2228571 Jan 04, 2002 (102)
rs17777794 Oct 08, 2004 (123)
rs17880019 Mar 11, 2006 (126)
rs59730659 May 25, 2008 (130)
rs118037316 Aug 16, 2010 (132)
rs386609145 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss89137833, ss160871589, ss175117861, ss198140414, ss208325743, ss210817036, ss211279905, ss244309162, ss286557561, ss481541541, ss491663924, ss1397633434, ss1599178741, ss1713325787, ss3642954991 NC_000012.10:46525023:A:G NC_000012.12:47844973:A:G (self)
57659016, 32018482, 22658701, 1167804, 157357155, 8991454, 1179500, 12284732, 32018482, 7109366, ss225741831, ss235926865, ss242488033, ss342354324, ss481570547, ss482543948, ss485565762, ss491040673, ss537462688, ss563151808, ss658704745, ss778600539, ss783228428, ss784182648, ss832488800, ss834057824, ss974483343, ss989508319, ss1067533218, ss1078444304, ss1344913977, ss1426926728, ss1576268438, ss1584081433, ss1628540160, ss1671534193, ss1690872933, ss1711328072, ss1752069124, ss1807234224, ss1932872881, ss1959431957, ss2027187806, ss2094793385, ss2095034753, ss2155523374, ss2353507935, ss2628073749, ss2632956191, ss2699866169, ss2739762403, ss2748852328, ss2910200516, ss2984973696, ss2985615942, ss3009644027, ss3021427636, ss3023067748, ss3350053056, ss3625622658, ss3626870894, ss3630965562, ss3633019492, ss3633720378, ss3634502637, ss3635411171, ss3636188350, ss3637162153, ss3637961234, ss3640209970, ss3646441402, ss3651804106, ss3651804107, ss3653746832, ss3676920453, ss3738999867, ss3744803327, ss3750449665, ss3772302817 NC_000012.11:48238756:A:G NC_000012.12:47844973:A:G (self)
RCV000361773.1, RCV000616832.1, 910217, 83237509, ss2189575466, ss3027402142, ss3170201336, ss3693619605, ss3725322219, ss3771688748, ss3815780035 NC_000012.12:47844973:A:G NC_000012.12:47844973:A:G (self)
ss12216651, ss14739713 NT_029419.10:10382062:A:G NC_000012.12:47844973:A:G (self)
ss76497, ss2420961, ss5586953, ss12568608, ss16359245, ss20420895, ss24395756, ss32465678, ss38908577, ss65743935, ss68316101, ss74882784, ss80755731, ss86241970, ss86343777, ss119365123, ss133153445, ss159726127, ss174334971, ss469996522 NT_029419.12:10382062:A:G NC_000012.12:47844973:A:G (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

309 citations for rs731236
PMID Title Author Year Journal
15113403 Current limitations of SNP data from the public domain for studies of complex disorders: a test for ten candidate genes for obesity and osteoporosis. Dvornyk V et al. 2004 BMC genetics
15157284 Patterns of linkage disequilibrium and haplotype distribution in disease candidate genes. Long JR et al. 2004 BMC genetics
15651992 Variants in the vitamin D receptor gene and asthma. Wjst M et al. 2005 BMC genetics
16279845 Vitamin D receptor polymorphisms are associated with Graves' disease in German and Polish but not in Serbian patients. Ramos-Lopez E et al. 2005 Thyroid
16600026 Asthma families show transmission disequilibrium of gene variants in the vitamin D metabolism and signalling pathway. Wjst M et al. 2006 Respiratory research
16634022 Polymorphisms in the vitamin D receptor and their associations with risk of schizophrenia and selected anthropometric measures. Handoko HY et al. 2006 American journal of human biology
16899094 The short vitamin D receptor is associated with increased risk for generalized aggressive periodontitis. Park KS et al. 2006 Journal of clinical periodontology
17135034 Polymorphisms of the vitamin D receptor gene predict the onset of surgical menopause in Caucasian females. Dvornyk V et al. 2006 Gynecological endocrinology
17244366 Vitamin D pathway gene polymorphisms, diet, and risk of postmenopausal breast cancer: a nested case-control study. McCullough ML et al. 2007 Breast cancer research
17867381 Vitamin D receptor gene (VDR) associations with cancer. Slattery ML et al. 2007 Nutrition reviews
17903296 Genome-wide association with bone mass and geometry in the Framingham Heart Study. Kiel DP et al. 2007 BMC medical genetics
17943423 Lack of association of VDR gene polymorphisms with thyroid autoimmune disorders: familial and case/control studies. Maalej A et al. 2008 Journal of clinical immunology
18079052 Vitamin D receptor polymorphisms and risk of epithelial ovarian cancer. Clendenen TV et al. 2008 Cancer letters
18086759 Vitamin D receptor gene polymorphisms and epithelial ovarian cancer risk. Lurie G et al. 2007 Cancer epidemiology, biomarkers & prevention
18086783 CDX2 VDR polymorphism and colorectal cancer. Slattery ML et al. 2007 Cancer epidemiology, biomarkers & prevention
18161000 Family-based analysis of vitamin D receptor gene polymorphisms and type 1 diabetes in the population of South Croatia. Boraska V et al. 2008 Journal of human genetics
18205735 Association of vitamin D receptor gene polymorphisms in Chinese patients with generalized aggressive periodontitis. Li S et al. 2008 Journal of periodontal research
18246496 Vitamin D receptor polymorphisms and renal cancer risk in Central and Eastern Europe. Karami S et al. 2008 Journal of toxicology and environmental health. Part A
18279374 Association of vitamin D receptor gene 3'-variants with Hashimoto's thyroiditis in the Croatian population. Stefanić M et al. 2008 International journal of immunogenetics
18316854 Analysis of vitamin D receptor gene polymorphisms in patients with chronic periodontitis. Gunes S et al. 2008 The Indian journal of medical research
18361940 Lack of association of vitamin D receptor gene polymorphisms with susceptibility to type 1 diabetes mellitus in the Portuguese population. Lemos MC et al. 2008 Human immunology
18419802 Vitamin D receptor gene polymorphisms and haplotypes and postmenopausal breast cancer risk. Abbas S et al. 2008 Breast cancer research
18587672 Vitamin D receptor variants and breast cancer risk in the Polish population. Gapska P et al. 2009 Breast cancer research and treatment
18628249 Association of vitamin D receptor gene variants, adiposity and colon cancer. Ochs-Balcom HM et al. 2008 Carcinogenesis
18705810 Analysis of association of clinical aspects and vitamin D receptor gene polymorphism with dental implant loss. Alvim-Pereira F et al. 2008 Clinical oral implants research
18849534 Association of genetic polymorphisms in vitamin D receptor gene and susceptibility to sporadic prostate cancer. Onen IH et al. 2008 Experimental biology and medicine (Maywood, N.J.)
18936436 Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994. Chang MH et al. 2009 American journal of epidemiology
19105801 Genetic analysis of the vitamin D receptor gene in two epithelial cancers: melanoma and breast cancer case-control studies. Barroso E et al. 2008 BMC cancer
19255064 Vitamin D-related genes, serum vitamin D concentrations and prostate cancer risk. Ahn J et al. 2009 Carcinogenesis
19383647 Past environmental sun exposure and risk of multiple sclerosis: a role for the Cdx-2 Vitamin D receptor variant in this interaction. Dickinson JL et al. 2009 Multiple sclerosis (Houndmills, Basingstoke, England)
19454612 Vitamin D pathway gene variants and prostate cancer risk. Holt SK et al. 2009 Cancer epidemiology, biomarkers & prevention
19499989 Vitamin D receptor polymorphisms in differentiated thyroid carcinoma. Penna-Martinez M et al. 2009 Thyroid
19584489 Vitamin D receptor (FokI, BsmI and TaqI) gene polymorphisms and type 2 diabetes mellitus: a North Indian study. Bid HK et al. 2009 Indian journal of medical sciences
19615888 Vitamin D receptor gene polymorphisms, serum 25-hydroxyvitamin D levels, and melanoma: UK case-control comparisons and a meta-analysis of published VDR data. Randerson-Moor JA et al. 2009 European journal of cancer (Oxford, England
19622139 Association study between vitamin D receptor gene polymorphisms and asthma in the Chinese Han population: a case-control study. Saadi A et al. 2009 BMC medical genetics
19644412 Polymorphisms in the vitamin D receptor gene and risk of lung cancer. Dogan I et al. 2009 Medical science monitor
19679055 Vitamin D receptor variants and the malignant melanoma risk: a population-based study. Gapska P et al. 2009 Cancer epidemiology
19682379 TagSNP transferability and relative loss of variability prediction from HapMap to an admixed population. Lins TC et al. 2009 Journal of biomedical science
19693091 Vitamin D receptor gene polymorphisms and distinct clinical phenotypes of hepatitis B carriers in Taiwan. Huang YW et al. 2010 Genes and immunity
19734102 Vitamin D receptor gene polymorphisms and susceptibility to type 1 diabetes in Crete, Greece. Panierakis C et al. 2009 Clinical immunology (Orlando, Fla.)
19753122 Analysis of SNPs and haplotypes in vitamin D pathway genes and renal cancer risk. Karami S et al. 2009 PloS one
19758194 Association study on two vitamin D receptor gene polymorphisms and vitamin D metabolites in multiple sclerosis. Smolders J et al. 2009 Annals of the New York Academy of Sciences
19770375 Serum 25-hydroxyvitamin D3 levels are associated with breslow thickness at presentation and survival from melanoma. Newton-Bishop JA et al. 2009 Journal of clinical oncology
19783860 A rare haplotype of the vitamin D receptor gene is protective against diabetic nephropathy. Martin RJ et al. 2010 Nephrology, dialysis, transplantation
19841454 Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture. Richards JB et al. 2009 Annals of internal medicine
19956101 Overview of the Rapid Response data. Brown WM et al. 2009 Genes and immunity
19956106 Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families. Howson JM et al. 2009 Genes and immunity
19956109 The Type I Diabetes Genetics Consortium 'Rapid Response' family-based candidate gene study: strategy, genes selection, and main outcome. Julier C et al. 2009 Genes and immunity
20006704 Lead and cognitive function in VDR genotypes in the third National Health and Nutrition Examination Survey. Krieg EF Jr et al. 2010 Neurotoxicology and teratology
20007432 Polymorphisms in vitamin D metabolism related genes and risk of multiple sclerosis. Simon KC et al. 2010 Multiple sclerosis (Houndmills, Basingstoke, England)
20009418 Matrix metalloproteinase-3 and vitamin d receptor genetic polymorphisms, and their interactions with occupational exposure in lumbar disc degeneration. Yuan HY et al. 2010 Journal of occupational health
20015871 Pharmacogenetic risk factors for altered bone mineral density and body composition in pediatric acute lymphoblastic leukemia. te Winkel ML et al. 2010 Haematologica
20023594 Bisphosphonates pathway. Gong L et al. 2011 Pharmacogenetics and genomics
20086113 Genetic variation in the vitamin D receptor (VDR) and the vitamin D-binding protein (GC) and risk for colorectal cancer: results from the Colon Cancer Family Registry. Poynter JN et al. 2010 Cancer epidemiology, biomarkers & prevention
20145122 Genetic polymorphisms in vitamin D receptor VDR/RXRA influence the likelihood of colon adenoma recurrence. Egan JB et al. 2010 Cancer research
20196868 Polymorphisms in IL-1beta, vitamin D receptor Fok1, and Toll-like receptor 2 are associated with extrapulmonary tuberculosis. Motsinger-Reif AA et al. 2010 BMC medical genetics
20357209 Molecular genetic studies of gene identification for osteoporosis: the 2009 update. Xu XH et al. 2010 Endocrine reviews
20565774 Population based allele frequencies of disease associated polymorphisms in the Personalized Medicine Research Project. Cross DS et al. 2010 BMC genetics
20585998 Variation in the vitamin D receptor gene is not associated with risk of colorectal cancer in the Czech Republic. Hughes DJ et al. 2011 Journal of gastrointestinal cancer
20650301 Association of TNF, MBL, and VDR polymorphisms with leprosy phenotypes. Sapkota BR et al. 2010 Human immunology
20687218 Vitamin D pathway gene variants and prostate cancer prognosis. Holt SK et al. 2010 The Prostate
20716226 Clinical and genetic predictors of response to narrowband ultraviolet B for the treatment of chronic plaque psoriasis. Ryan C et al. 2010 The British journal of dermatology
20961463 Genetic predisposition for femoral neck stress fractures in military conscripts. Korvala J et al. 2010 BMC genetics
21054877 Inflammation gene variants and susceptibility to albuminuria in the U.S. population: analysis in the Third National Health and Nutrition Examination Survey (NHANES III), 1991-1994. Ned RM et al. 2010 BMC medical genetics
21076051 Vitamin D receptor genotypes, ultraviolet radiation exposure, and risk of non-Hodgkin lymphoma. Smedby KE et al. 2011 American journal of epidemiology
21082232 Influence of gene variants related to calcium homeostasis on biochemical parameters of women with polycystic ovary syndrome. Ranjzad F et al. 2011 Journal of assisted reproduction and genetics
21168462 Vitamin D receptor gene methylation is associated with ethnicity, tuberculosis, and TaqI polymorphism. Andraos C et al. 2011 Human immunology
21198767 BsmI, TaqI, ApaI, and FokI polymorphisms in the vitamin D receptor gene and periodontitis: a meta-analysis of 15 studies including 1338 cases and 1302 controls. Deng H et al. 2011 Journal of clinical periodontology
21309754 Vitamin D receptor gene as a candidate gene for Parkinson disease. Butler MW et al. 2011 Annals of human genetics
21358824 Prostate cancer susceptibility Loci identified on chromosome 12 in African Americans. Bonilla C et al. 2011 PloS one
21365644 Vitamin D receptor polymorphisms in patients with cutaneous melanoma. Orlow I et al. 2012 International journal of cancer
21514219 Genetic variants associated with breast-cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence. Zhang B et al. 2011 The Lancet. Oncology
21537388 Genetic risk factors of disc degeneration among 12-14-year-old Danish children: a population study. Eskola PJ et al. 2010 International journal of molecular epidemiology and genetics
21545713 Vitamin D receptor gene polymorphisms in multiple sclerosis patients in northwest Greece. Sioka C et al. 2011 Journal of negative results in biomedicine
21548019 Maternal vitamin D receptor genetic variation contributes to infant birthweight among black mothers. Swamy GK et al. 2011 American journal of medical genetics. Part A
21613960 Associations between genetic variants in vitamin D metabolism and asthma characteristics in young African Americans: a pilot study. Pillai DK et al. 2011 Journal of investigative medicine
21664963 Vitamin D receptor (VDR) gene SNPs influence VDR expression and modulate protection from multiple sclerosis in HLA-DRB1*15-positive individuals. Agliardi C et al. 2011 Brain, behavior, and immunity
21814771 Coding region analysis of vitamin D receptor gene and its association with active calcium stone disease. Basiri A et al. 2012 Urological research
21818054 Common variation in the vitamin D receptor gene and risk of inflammatory bowel disease in an Irish case-control study. Hughes DJ et al. 2011 European journal of gastroenterology & hepatology
21828234 Common genetic variants in the vitamin D pathway including genome-wide associated variants are not associated with breast cancer risk among Chinese women. Dorjgochoo T et al. 2011 Cancer epidemiology, biomarkers & prevention
21918647 Pathway-Targeted Pharmacogenomics of CYP1A2 in Human Liver. Klein K et al. 2010 Frontiers in pharmacology
21931507 Population analysis of vitamin D receptor polymorphisms and the role of genetic ancestry in an admixed population. Lins TC et al. 2011 Genetics and molecular biology
21951018 Lack of association of vitamin D receptor gene 3'-haplotypes with psoriasis in Croatian patients. Rucevic I et al. 2012 The Journal of dermatology
22008758 SLC11A1 and VDR gene variants and susceptibility to tuberculosis and disease progression in East India. Singh A et al. 2011 The international journal of tuberculosis and lung disease
22022386 Case-control study of vitamin D, dickkopf homolog 1 (DKK1) gene methylation, VDR gene polymorphism and the risk of colon adenoma in African Americans. Ashktorab H et al. 2011 PloS one
22024213 A novel gene-environment interaction involved in endometriosis. McCarty CA et al. 2012 International journal of gynaecology and obstetrics
22037866 Genes and the ageing muscle: a review on genetic association studies. Garatachea N et al. 2013 Age (Dordrecht, Netherlands)
22046258 Genetic associations in the vitamin D receptor and colorectal cancer in African Americans and Caucasians. Kupfer SS et al. 2011 PloS one
22110781 Vitamin D receptor (VDR) polymorphisms and skin cancer: A systematic review. Denzer N et al. 2011 Dermato-endocrinology
22151003 Combined effect of 25-OH vitamin D plasma levels and genetic vitamin D receptor (NR 1I1) variants on fibrosis progression rate in HCV patients. Baur K et al. 2012 Liver international
22155603 Systems biology-based analysis implicates a novel role for vitamin D metabolism in the pathogenesis of age-related macular degeneration. Morrison MA et al. 2011 Human genomics
22170372 Vitamin D receptor and megalin gene polymorphisms and their associations with longitudinal cognitive change in US adults. Beydoun MA et al. 2012 The American journal of clinical nutrition
22213340 25-hydroxyvitamin D, vitamin D receptor gene polymorphisms, and severity of Parkinson's disease. Suzuki M et al. 2012 Movement disorders
22219324 Vitamin D receptor gene polymorphisms and HLA DRB1*04 cosegregation in Saudi type 2 diabetes patients. Al-Daghri NM et al. 2012 Journal of immunology (Baltimore, Md.
22242137 Prognostic significance of vitamin D receptor polymorphisms in head and neck squamous cell carcinoma. Hama T et al. 2011 PloS one
22311020 Evaluation of ERα and VDR gene polymorphisms in relation to bone mineral density in Turkish postmenopausal women. Kurt O et al. 2012 Molecular biology reports
22422157 Vitamin D receptor gene variability as a factor influencing bone mineral density in pediatric patients. Jakubowska-Pietkiewicz E et al. 2012 Molecular biology reports
22480149 Variants in the vitamin D pathway, serum levels of vitamin D, and estrogen receptor negative breast cancer among African-American women: a case-control study. Yao S et al. 2012 Breast cancer research
22500139 Host genetic susceptibility to severe dengue infection. Lan NT et al. 2011 Tropical medicine and health
22522591 Genetic variations in bile acid homeostasis are not overrepresented in alcoholic cirrhosis compared to patients with heavy alcohol abuse and absent liver disease. Many N et al. 2012 Mutagenesis
22523693 Nuclear receptor variants in liver disease. Müllenbach R et al. 2012 Journal of lipids
22550553 An Association Study of Interleukin 18 Receptor Genes (IL18R1 and IL18RAP) in Lumbar Disc Degeneration. Omair A et al. 2012 The open orthopaedics journal
22551951 Allelic variations in the vitamin D receptor gene, insulin secretion and parents' heights are independently associated with height in obese children and adolescents. Ferrarezi DA et al. 2012 Metabolism
22576141 No association of vitamin D metabolism-related polymorphisms and melanoma risk as well as melanoma prognosis: a case-control study. Schäfer A et al. 2012 Archives of dermatological research
22672495 Vitamin D3 receptor is highly expressed in Hodgkin's lymphoma. Renné C et al. 2012 BMC cancer
22681928 Vitamin D deficiency in girls from South Brazil: a cross-sectional study on prevalence and association with vitamin D receptor gene variants. Santos BR et al. 2012 BMC pediatrics
22690210 Vitamin d receptor polymorphisms predispose to primary biliary cirrhosis and severity of the disease in polish population. Kempińska-Podhorecka A et al. 2012 Gastroenterology research and practice
22726649 25-hydroxyvitamin D deficiency, exacerbation frequency and human rhinovirus exacerbations in chronic obstructive pulmonary disease. Quint JK et al. 2012 BMC pulmonary medicine
22740028 An exploratory analysis of common genetic variants in the vitamin D pathway including genome-wide associated variants in relation to glioma risk and outcome. Anic GM et al. 2012 Cancer causes & control
22917542 Association of vitamin D receptor gene polymorphisms with clinical outcomes of dengue virus infection. Alagarasu K et al. 2012 Human immunology
22947263 Association study between vitamin d receptor gene polymorphisms and patients with Parkinson disease in Chinese Han population. Lv Z et al. 2013 The International journal of neuroscience
23034014 Association of vitamin D receptor gene polymorphisms with severe atopic dermatitis in adults. Heine G et al. 2013 The British journal of dermatology
23050050 Gender difference in genetic association between IL1A variant and early lumbar disc degeneration: a three-year follow-up. Eskola PJ et al. 2012 International journal of molecular epidemiology and genetics
23065277 Vitamin D receptor gene BsmI, FokI, ApaI and TaqI polymorphisms and the risk of systemic lupus erythematosus. Mostowska A et al. 2013 Molecular biology reports
23065592 Polymorphisms in the vitamin D receptor gene and risk of autoimmune thyroid diseases: a meta-analysis. Feng M et al. 2013 Endocrine
23070913 Association of vitamin D binding protein polymorphism with long-term kidney allograft survival in Hispanic kidney transplant recipients. Vu D et al. 2013 Molecular biology reports
23103831 VDR TaqI is associated with obesity in the Greek population. Vasilopoulos Y et al. 2013 Gene
23185470 Vitamin D in a northern Canadian first nation population: dietary intake, serum concentrations and functional gene polymorphisms. Larcombe L et al. 2012 PloS one
23209686 Vitamin D receptor gene and aggrecan gene polymorphisms and the risk of intervertebral disc degeneration - a meta-analysis. Xu G et al. 2012 PloS one
23300018 Vitamin D receptor genotype rs731236 (Taq1) and breast cancer prognosis. Perna L et al. 2013 Cancer epidemiology, biomarkers & prevention
23459936 Exploring the genetic basis of chronic periodontitis: a genome-wide association study. Divaris K et al. 2013 Human molecular genetics
23467735 Plasma Vitamin D Levels And Vitamin D Receptor Polymorphisms Are Associated with Survival of Non-small Cell Lung Cancer. Liu Y et al. 2011 Chinese journal of cancer research = Chung-kuo yen cheng yen chiu
23639864 Otosclerosis and vitamin D receptor gene polymorphism. Yıldırım YS et al. 2013 American journal of otolaryngology
23841669 VDR gene polymorphisms, interaction with smoking and risk of periodontal disease in Japanese women: the Kyushu Okinawa maternal and child health study. Tanaka K et al. 2013 Scandinavian journal of immunology
23975234 Vitamin D receptor (VDR) gene polymorphism influences the risk of osteoporosis in postmenopausal women of Northwest India. Singh M et al. 2013 Archives of osteoporosis
24019226 Vitamin D receptor (VDR) polymorphisms and severe RSV bronchiolitis: a systematic review and meta-analysis. McNally JD et al. 2014 Pediatric pulmonology
24075799 Vitamin D receptor polymorphism and colorectal cancer-specific and all-cause mortality. Perna L et al. 2013 Cancer epidemiology
24078159 Genetic variation in the vitamin D receptor gene and vitamin D serum levels in Egyptian women with polycystic ovary syndrome. El-Shal AS et al. 2013 Molecular biology reports
24084050 The role of Vitamin D level and related single nucleotide polymorphisms in Crohn's disease. Carvalho AY et al. 2013 Nutrients
24149131 Candidate gene analysis in israeli soldiers with stress fractures. Yanovich R et al. 2012 Journal of sports science & medicine
24224838 Polymorphisms in the vitamin D receptor gene and risk of primary biliary cirrhosis: a meta-analysis. Li YJ et al. 2014 Journal of gastroenterology and hepatology
24336386 Vitamin D receptor gene polymorphisms and the risk of rickets among Asians: a meta-analysis. Mao S et al. 2014 Archives of disease in childhood
24415299 Juvenile idiopathic arthritis patients and their skeletal status: possible role of vitamin D receptor gene polymorphism. Kostik MM et al. 2014 Molecular biology reports
24497837 Comprehensive functional annotation of 77 prostate cancer risk loci. Hazelett DJ et al. 2014 PLoS genetics
24517634 Staphylococcus aureus nasal carriage might be associated with vitamin D receptor polymorphisms in type 2 diabetes. Messaritakis I et al. 2014 Clinical microbiology and infection
24597698 Tumour necrosis factor-alpha, interleukin-10, interferon-gamma and vitamin D receptor gene polymorphisms in patients with chronic hepatitis delta. Karatayli SC et al. 2014 Journal of viral hepatitis
24653663 Systemic Lupus Erythematosus: Old and New Susceptibility Genes versus Clinical Manifestations. J de AS et al. 2014 Current genomics
24681889 The common occurrence of epistasis in the determination of human pigmentation and its impact on DNA-based pigmentation phenotype prediction. Pośpiech E et al. 2014 Forensic science international. Genetics
24755043 Kallikrein 3 and vitamin D receptor polymorphisms: potentials environmental risk factors for prostate cancer. Hu J et al. 2014 Diagnostic pathology
24755231 NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis. Agúndez JA et al. 2014 BMC neurology
24769568 Association between vitamin D receptor gene polymorphisms and breast cancer risk: a meta-analysis of 39 studies. Zhang K et al. 2014 PloS one
24840096 Association of vitamin D receptor gene polymorphism with the risk of renal cell carcinoma: a meta-analysis. Ou C et al. 2014 Journal of receptor and signal transduction research
24875270 Association of vitamin D receptor gene polymorphism with the risk of lung cancer: a meta-analysis. Zhong H et al. 2014 Journal of receptor and signal transduction research
24894441 Significance of vitamin d receptor gene polymorphisms for risk of hepatocellular carcinoma in chronic hepatitis C. Hung CH et al. 2014 Translational oncology
24927719 Interrelation between genotypes of the vitamin D receptor gene and serum sex hormone concentrations in the Polish elderly population: the PolSenior study. Laczmanski L et al. 2014 Experimental gerontology
24971027 Vitamin D and inflammatory diseases. Yin K et al. 2014 Journal of inflammation research
24996287 Association of vitamin D receptor FokI and ApaI polymorphisms with lung cancer risk in Tunisian population. Kaabachi W et al. 2014 Molecular biology reports
25000366 Association of vitamin D receptor gene polymorphism with the urine calcium level in nephrolithiasis patients. Zhou TB et al. 2015 Journal of receptor and signal transduction research
25020064 Vitamin D receptor gene polymorphisms are associated with obesity and inflammosome activity. Al-Daghri NM et al. 2014 PloS one
25046415 The functional polymorphisms of VDR, GC and CYP2R1 are involved in the pathogenesis of autoimmune thyroid diseases. Inoue N et al. 2014 Clinical and experimental immunology
25051494 Association of vitamin D receptor BsmI (rs1544410), Fok1 (rs2228570), TaqI (rs731236) and ApaI (rs7975232) gene polymorphism with the nephrolithiasis susceptibility. Zhou TB et al. 2015 Journal of receptor and signal transduction research
25347090 VDR polymorphisms are associated with bone mineral density in post-menopausal Mayan-Mestizo women. Canto-Cetina T et al. 2015 Annals of human biology
25347331 Association of vitamin D receptor gene polymorphisms with the susceptibility to ulcerative colitis in patients from Southeast China. Xia SL et al. 2015 Journal of receptor and signal transduction research
25421379 Vitamin D-related gene polymorphisms, plasma 25-hydroxyvitamin D, and breast cancer risk. Reimers LL et al. 2015 Cancer causes & control
25448747 Immunomodulatory effects of 25-hydroxyvitamin D3 on monocytic cell differentiation and influence of vitamin D3 polymorphisms in type 1 diabetes. Mauf S et al. 2015 The Journal of steroid biochemistry and molecular biology
25587543 T-cell cytokine gene polymorphisms and vitamin D pathway gene polymorphisms in end-stage renal disease due to type 2 diabetes mellitus nephropathy: comparisons with health status and other main causes of end-stage renal disease. Grzegorzewska AE et al. 2014 Journal of diabetes research
25595352 Association between vitamin D concentration and levels of sex hormones in an elderly Polish population with different genotypes of VDR polymorphisms (rs10735810, rs1544410, rs7975232, rs731236). Laczmanski L et al. 2015 Gene
25661837 Association between vitamin D receptor (VDR) gene polymorphisms and systemic lupus erythematosus in Portuguese patients. Carvalho C et al. 2015 Lupus
25738688 Meta-analysis on vitamin D receptor and cancer risk: focus on the role of TaqI, ApaI, and Cdx2 polymorphisms. Serrano D et al. 2016 European journal of cancer prevention
25817800 Association between FokI, ApaI and TaqI RFLP polymorphisms in VDR gene and Hashimoto's thyroiditis: preliminary data from female patients in Serbia. Djurovic J et al. 2015 International journal of immunogenetics
25890641 Vitamin D receptor gene polymorphisms and Parkinson's disease in a population with high ultraviolet radiation exposure. Gatto NM et al. 2015 Journal of the neurological sciences
25945350 Variants of SCARB1 and VDR Involved in Complex Genetic Interactions May Be Implicated in the Genetic Susceptibility to Clear Cell Renal Cell Carcinoma. Pośpiech E et al. 2015 BioMed research international
26093050 Vitamin D receptor gene polymorphisms in Alzheimer's disease patients. Łaczmański Ł et al. 2015 Experimental gerontology
26107257 Polymorphisms in CaSR and CLDN14 Genes Associated with Increased Risk of Kidney Stone Disease in Patients from the Eastern Part of India. Guha M et al. 2015 PloS one
26109216 Maternal VDR variants rather than 25-hydroxyvitamin D concentration during early pregnancy are associated with type 1 diabetes in the offspring. Miettinen ME et al. 2015 Diabetologia
26141257 Low vitamin D status is associated with more depressive symptoms in Dutch older adults. Brouwer-Brolsma EM et al. 2016 European journal of nutrition
26177022 Association of VDR and CYP2R1 Polymorphisms with Mite-Sensitized Persistent Allergic Rhinitis in a Chinese Population. Tian HQ et al. 2015 PloS one
26193879 Genotype-independent association between profound vitamin D deficiency and delayed sputum smear conversion in pulmonary tuberculosis. Junaid K et al. 2015 BMC infectious diseases
26219465 Influence of ethnicity on the distribution of genetic polymorphisms associated with risk of chronic liver disease in South American populations. Pontoriero AC et al. 2015 BMC genetics
26284412 [Relationship between vitamin D receptor gene polymorphisms and chronic periodontitis]. Cao XJ et al. 2015 Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences
26303648 Association of vdr, cyp27b1, cyp24a1 and mthfr gene polymorphisms with oral lichen planus risk. Kujundzic B et al. 2016 Clinical oral investigations
26346690 Association of vitamin D receptor gene polymorphisms and vitamin D levels with asthma and atopy in Cypriot adolescents: a case-control study. Papadopoulou A et al. 2015 Multidisciplinary respiratory medicine
26379431 Association between vitamin D receptor polymorphisms and osteoporosis in patients with COPD. Kim SW et al. 2015 International journal of chronic obstructive pulmonary disease
26422783 Classic PCOS phenotype is not associated with deficiency of endogenous vitamin D and VDR gene polymorphisms rs731236 (TaqI), rs7975232 (ApaI), rs1544410 (BsmI), rs10735810 (FokI): a case-control study of lower Silesian women. Jedrzejuk D et al. 2015 Gynecological endocrinology
26423691 Low Vitamin D Levels and Genetic Polymorphism in the Vitamin D Receptor are Associated with Increased Risk of Statin-Induced Myopathy. Ovesjö ML et al. 2016 Basic & clinical pharmacology & toxicology
26504744 Frequency of rs731236 (Taql), rs2228570 (Fok1) of Vitamin-D Receptor (VDR) gene in Emirati healthy population. Osman E et al. 2015 Meta gene
26521212 Vitamin D receptor polymorphisms and survival in patients with cutaneous melanoma: a population-based study. Orlow I et al. 2016 Carcinogenesis
26556986 Genetic, metabolic and environmental factors involved in the development of liver cirrhosis in Mexico. Ramos-Lopez O et al. 2015 World journal of gastroenterology
26643661 Preliminary evaluation of exome sequencing to identify genetic markers of susceptibility to tuberculosis disease. Duncan C et al. 2015 BMC research notes
26699871 Genetic Variations in the Vitamin D Receptor Predict Type 2 Diabetes and Myocardial Infarction in a Community-Based Population: The Tromsø Study. Zostautiene I et al. 2015 PloS one
26718096 Lipids, blood pressure and kidney update 2015. Banach M et al. 2015 Lipids in health and disease
26724524 Vitamin D receptor GATG haplotype association with atherosclerotic disease in patients with rheumatoid arthritis. López-Mejías R et al. 2016 Atherosclerosis
26742922 Association Between Vitamin D Receptor Polymorphism and Familial Mediterranean Fever Disease in Turkish Children. Kizildag S et al. 2016 Biochemical genetics
26756741 Systematic Review of the Relationship between Vitamin D and Parkinson's Disease. Rimmelzwaan LM et al. 2016 Journal of Parkinson's disease
26772150 Association Between VDR FokI Polymorphism and Intervertebral Disk Degeneration. Zhao J et al. 2015 Genomics, proteomics & bioinformatics
26784653 Association between vitamin D receptor ApaI and TaqI gene polymorphisms and gestational diabetes mellitus in an Iranian pregnant women population. Rahmannezhad G et al. 2016 Gene
26793196 Gene Association with Leprosy: A Review of Published Data. Mazini PS et al. 2015 Frontiers in immunology
26798662 Genetic Factors in Systemic Lupus Erythematosus: Contribution to Disease Phenotype. Ceccarelli F et al. 2015 Journal of immunology research
26815041 Associations between vitamin D receptor gene polymorphisms and ankylosing spondylitis in Chinese Han population: a case-control study. Cai G et al. 2016 Osteoporosis international
26868429 Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis. Agúndez JA et al. 2016 Scientific reports
26872154 Low Vitamin-D Levels Combined with PKP3-SIGIRR-TMEM16J Host Variants Is Associated with Tuberculosis and Death in HIV-Infected and -Exposed Infants. Gupta A et al. 2016 PloS one
26881316 Independent associations of polymorphisms in vitamin D binding protein (GC) and vitamin D receptor (VDR) genes with obesity and plasma 25OHD3 levels demonstrate sex dimorphism. Almesri N et al. 2016 Applied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme
26911666 Integrative role of vitamin D related and Interleukin-28B genes polymorphism in predicting treatment outcomes of Chronic Hepatitis C. El-Derany MO et al. 2016 BMC gastroenterology
26921301 Latitudinal Clines of the Human Vitamin D Receptor and Skin Color Genes. Tiosano D et al. 2016 G3 (Bethesda, Md.)
26945655 Association of the BsmI, ApaI, TaqI, Tru9I and FokI Polymorphisms of the Vitamin D Receptor Gene with Nephrolithiasis in the Turkish Population. Cakir OO et al. 2016 Urology journal
26967244 Systematic meta-analyses of gene-specific genetic association studies in prostate cancer. Hao Q et al. 2016 Oncotarget
27018192 Role of vitamin D receptor gene polymorphisms in aplastic anemia: a case-control study from China. Yu W et al. 2016 International journal of laboratory hematology
27066374 Association of vitamin D receptor variants with clinical parameters in prostate cancer. Nunes SB et al. 2016 SpringerPlus
27088875 Vitamin D receptor polymorphisms may contribute to asthma risk. Han JC et al. 2016 The Journal of asthma
27114922 Vitamin D receptor gene polymorphism in Egyptian pediatric acute lymphoblastic leukemia correlation with BMD. Tantawy M et al. 2016 Meta gene
27124026 25-Hydroxy Vitamin D, Vitamin D Receptor and Toll-like Receptor 2 Polymorphisms in Spinal Tuberculosis: A Case-Control Study. Panwar A et al. 2016 Medicine
27149110 BsmI, ApaI and TaqI Polymorphisms in the Vitamin D Receptor Gene (VDR) and Association with Lumbar Spine Pathologies: An Italian Case-Control Study. Colombini A et al. 2016 PloS one
27149457 Vitamin D Receptor Polymorphism and Breast Cancer Risk: A Meta-Analysis. Lu D et al. 2016 Medicine
27160686 Vitamin D deficiency associates with susceptibility to tuberculosis in Pakistan, but polymorphisms in VDR, DBP and CYP2R1 do not. Junaid K et al. 2016 BMC pulmonary medicine
27174575 The vitamin D receptor gene ApaI polymorphism is associated with increased risk of renal cell carcinoma in Chinese population. Yang C et al. 2016 Scientific reports
27175669 The Association Between Genetic Polymorphism rs703842 in CYP27B1 and Multiple Sclerosis: A Meta-Analysis. Jiang T et al. 2016 Medicine
27186331 Prevalence of common vitamin D receptor gene polymorphisms in HIV-infected and uninfected South Africans. McNamara L et al. 2016 International journal of molecular epidemiology and genetics
27309378 Association of Vitamin D Receptor Gene Polymorphisms with Colorectal Cancer in a Saudi Arabian Population. Alkhayal KA et al. 2016 PloS one
27345382 Vitamin D receptor polymorphisms and Parkinson's disease in a Korean population: Revisited. Kang SY et al. 2016 Neuroscience letters
27435453 Associations of vitamin D deficiency and vitamin D receptor (Cdx-2, Fok I, Bsm I and Taq I) polymorphisms with the risk of primary open-angle glaucoma. Lv Y et al. 2016 BMC ophthalmology
27446548 Association between the vitamin D receptor gene polymorphism and osteoporosis. Wu J et al. 2016 Biomedical reports
27468225 Pharmacogenetic analysis of cinacalcet response in secondary hyperparathyroidism patients. Jeong S et al. 2016 Drug design, development and therapy
27502545 Evaluation of VDR gene polymorphisms in Trypanosoma cruzi infection and chronic Chagasic cardiomyopathy. Leon Rodriguez DA et al. 2016 Scientific reports
27536155 The association between vitamin D receptor gene polymorphisms (TaqI and FokI), Type 2 diabetes, and micro-/macrovascular complications in postmenopausal women. Maia J et al. 2016 The application of clinical genetics
27551963 Association of vitamin D receptor gene polymorphisms with susceptibility to childhood asthma: A meta-analysis. Zhao DD et al. 2017 Pediatric pulmonology
27584680 Lead-Related Genetic Loci, Cumulative Lead Exposure and Incident Coronary Heart Disease: The Normative Aging Study. Ding N et al. 2016 PloS one
27589735 A Genomics-Based Model for Prediction of Severe Bioprosthetic Mitral Valve Calcification. Ponasenko AV et al. 2016 International journal of molecular sciences
27613009 Vitamin D receptor gene polymorphisms and lumbar disc degeneration: a systematic review and meta-analysis. Jiang H et al. 2017 European spine journal
27639591 Evidence for epistatic interaction between VDR and SLC13A2 genes in the pathogenesis of hypocitraturia in recurrent calcium oxalate stone formers. Rendina D et al. 2017 Journal of nephrology
27669215 Vitamin D-Related Gene Polymorphisms, Plasma 25-Hydroxy-Vitamin D, Cigarette Smoke and Non-Small Cell Lung Cancer (NSCLC) Risk. Wu X et al. 2016 International journal of molecular sciences
27672714 Relationship between vitamin D receptor gene polymorphisms, cardiovascular risk factors and adiponectin in a healthy young population. Hajj A et al. 2016 Pharmacogenomics
27688524 TaqI, FokI, and ApaI Polymorphisms in the Vitamin D Receptor in Behçet's Disease in Turkish Population. Erten G et al. 2016 Disease markers
27698765 Association of genetic polymorphisms of GALNT3 and VDR with osteoporosis in postmenopausal women. Wang G et al. 2016 Experimental and therapeutic medicine
27736940 Vitamin D Receptor Gene Polymorphism and the Risk of Colorectal Cancer: A Nested Case-Control Study. Budhathoki S et al. 2016 PloS one
27763570 Vitamin D Status and Its Consequences for Health in South Africa. Norval M et al. 2016 International journal of environmental research and public health
27778467 Association between vitamin D receptor gene polymorphism and ankylosing spondylitis in Han Chinese. Zhang P et al. 2017 International journal of rheumatic diseases
27790329 Vitamin D Receptor Gene, Matrix Metalloproteinase 3 Polymorphisms and the Risk of Intervertebral Disc Degeneration Susceptibility: Meta-Analysis. Nong L et al. 2016 Asian spine journal
27833587 A Candidate Gene Association Study of Bone Mineral Density in an Iranian Population. Dastgheib SA et al. 2016 Frontiers in endocrinology
27889775 Vitamin D Receptor TaqI Gene Polymorphism and Dental Caries in Czech Children. Izakovicova Holla L et al. 2017 Caries research
27891515 The Association between VDR Gene Polymorphisms and Diabetic Retinopathy Susceptibility: A Systematic Review and Meta-Analysis. Zhang Y et al. 2016 BioMed research international
27917384 Genetic Alterations in Intervertebral Disc Disease. Martirosyan NL et al. 2016 Frontiers in surgery
28216333 Vitamin D receptor gene polymorphisms, smoking, and risk of sporadic Parkinson's disease in Japan. Tanaka K et al. 2017 Neuroscience letters
28222630 Association of VDR polymorphisms ( Taq I and Bsm I) with prostate cancer: a new meta-analysis. Liu S et al. 2017 The Journal of international medical research
28228780 The relationship between vitamin D receptor (VDR) polymorphism and the occurrence of osteoporosis in menopausal Iranian women. Dabirnia R et al. 2016 Clinical cases in mineral and bone metabolism
28262345 Influence of NR3C1 and VDR polymorphisms on stable warfarin dose in patients with mechanical cardiac valves. Lee KE et al. 2017 International journal of cardiology
28285414 A population association study of vitamin D receptor gene polymorphisms and haplotypes with the risk of systemic lupus erythematosus in a Chinese population. Chen XE et al. 2017 Immunologic research
28323045 Vitamin D receptor gene polymorphisms among Emirati patients with type 2 diabetes mellitus. Safar HA et al. 2018 The Journal of steroid biochemistry and molecular biology
28361944 Association Study of Reported Significant Loci at 5q35.3, 7p14.3, 13q14.1 and 16p12.3 with Urolithiasis in Chinese Han Ethnicity. Wang L et al. 2017 Scientific reports
28384983 Association Study of Vitamin D Receptor (VDR) - Related Genetic Polymorphisms and their Haplotypes with Chronic Periodontitis in Colombian Population. Tobón-Arroyave SI et al. 2017 Journal of clinical and diagnostic research
28385183 Vitamin D receptor gene polymorphisms are associated with multiple sclerosis in Mexican adults. Bermúdez-Morales VH et al. 2017 Journal of neuroimmunology
28411367 Serum 25(OH)D concentration, common variants of the VDR gene and lung cancer occurrence. Gromowski T et al. 2017 International journal of cancer
28426778 ApaI polymorphism of vitamin D receptor affects health-related quality of life in patients with primary sclerosing cholangitis. Kempinska-Podhorodecka A et al. 2017 PloS one
28446629 Vitamin D Receptor and Megalin Gene Polymorphisms Are Associated with Longitudinal Cognitive Change among African-American Urban Adults. Beydoun MA et al. 2017 The Journal of nutrition
28469103 Association between Serum 25-hydroxy Vitamin D Concentration and <i>TaqI</i> Vitamin D Receptor Gene Polymorphism among Jordanian Females with Breast Cancer. Atoum MF et al. 2017 Chinese medical journal
28471875 Genetic predictors of recovery in low back and lumbar radicular pain. Bjorland S et al. 2017 Pain
28527290 Association of polymorphic variants of PTPN22, TNF and VDR genes in children with lupus nephritis: A study in Colombian family triads. Garavito G et al. 2017 Biomedica
28607807 Immunohistochemical evaluation of vitamin D receptor (VDR) expression in cutaneous melanoma tissues and four VDR gene polymorphisms. La Marra F et al. 2017 Cancer biology & medicine
28822353 VDR Gene variation and insulin resistance related diseases. Han FF et al. 2017 Lipids in health and disease
28851298 Vitamin D receptor gene polymorphisms in association with diabetic nephropathy: a systematic review and meta-analysis. Yang L et al. 2017 BMC medical genetics
28868946 Vitamin D receptor gene polymorphisms and risk of polycystic ovary syndrome in South Indian women. Siddamalla S et al. 2018 Gynecological endocrinology
29022486 Association of vitamin D receptor gene polymorphisms with breast cancer risk in an Egyptian population. El-Shorbagy HM et al. 2017 Tumour biology
29033051 Genetics of restless legs syndrome: An update. Jiménez-Jiménez FJ et al. 2018 Sleep medicine reviews
29100280 Impact of phosphoinositide-3-kinase and vitamin D3 nuclear receptor single-nucleotide polymorphisms on the outcome of malignant melanoma patients. Morgese F et al. 2017 Oncotarget
29129460 The association of novel polymorphisms with stress fracture injury in Elite Athletes: Further insights from the SFEA cohort. Varley I et al. 2018 Journal of science and medicine in sport
29331875 The association between vitamin D receptor polymorphisms and multiple sclerosis in a Turkish population. Kamisli O et al. 2018 Multiple sclerosis and related disorders
29333433 Vitamin D Receptor Gene Polymorphisms Influence T1D Susceptibility among Pakistanis. Mukhtar M et al. 2017 International journal of genomics
29351807 Vitamin D receptor rs2228570 polymorphism is associated with LH levels in men exposed to anabolic androgenic steroids. Björkhem-Bergman L et al. 2018 BMC research notes
29384117 Vitamin D receptor variants and uncontrolled asthma. Hutchinson K et al. 2018 European annals of allergy and clinical immunology
29399716 Pharmacogenetics of post-transplant diabetes mellitus in children with renal transplantation treated with tacrolimus. Lancia P et al. 2018 Pediatric nephrology (Berlin, Germany)
29409002 PTPN22 and CTLA-4 Polymorphisms Are Associated With Polyglandular Autoimmunity. Houcken J et al. 2018 The Journal of clinical endocrinology and metabolism
29465575 Impact of vitamin D receptor and binding protein gene polymorphisms in clinical and laboratory data of HCV patients: Cross sectional study. Scalioni LP et al. 2018 Medicine
29530503 Vitamin D deficiency and vitamin D receptor variants in mothers and their neonates are risk factors for neonatal sepsis. Tayel SI et al. 2018 Steroids
29544394 Association of vitamin D receptor gene TaqI, FokI and ApaI variants with arteriovenous fistula failure in hemodialysis patients. Huzmeli C et al. 2018 The journal of vascular access
29549381 Polymorphisms of the VDR gene in patients with nephrolithiasis in a Han Chinese population. Yang Z et al. 2019 Urolithiasis
29622662 Potential genetic polymorphisms predicting polycystic ovary syndrome. Chen Y et al. 2018 Endocrine connections
29669566 Apa-I polymorphism in VDR gene is related to metabolic syndrome in polycystic ovary syndrome: a cross-sectional study. Santos BR et al. 2018 Reproductive biology and endocrinology
29765404 Meta-Analysis of the Association between Vitamin D Receptor Polymorphisms and the Risk of Autoimmune Thyroid Disease. Gao XR et al. 2018 International journal of endocrinology
29788141 A Single Nucleotide Polymorphism in the Vitamin D Receptor Gene Is Associated With Decreased Levels of the Protein and a Penetrating Pattern in Crohn's Disease. Gisbert-Ferrándiz L et al. 2018 Inflammatory bowel diseases
29795187 Vitamin D Metabolism-Related Gene Haplotypes and Their Association with Metabolic Disturbances Among African-American Urban Adults. Beydoun MA et al. 2018 Scientific reports
29805861 Vitamin D Receptor Gene Polymorphisms in Susceptibility to Tuberculosis in the Kazakh Population in Almaty and Almaty Area. Zhabagin M et al. 2013 Central Asian journal of global health
29911037 Prevalence Pattern of Key Polymorphisms in the Vitamin D Receptor gene among Patients of Type 2 Diabetes Mellitus in Northeast India. Sarma D et al. 2018 Indian journal of endocrinology and metabolism
29922235 Association of Vitamin D Receptor Gene Variation With Osteoporosis Risk in Belarusian and Lithuanian Postmenopausal Women. Marozik PM et al. 2018 Frontiers in endocrinology
29926136 Association between vitamin D receptor gene polymorphisms and idiopathic hypocitraturia in a Chinese Bai population. Li K et al. 2019 Urolithiasis
29970659 Relationship between Vitamin D receptor gene polymorphism and renal cell carcinoma susceptibility. Lin ZJ et al. 2018 Journal of cancer research and therapeutics
29972092 Variability of contribution of vitamin D receptor gene polymorphisms to outcome of HLA-matched sibling allogeneic bone marrow transplantation. Kamel AM et al. 2018 Leukemia & lymphoma
30083974 Association of vitamin D binding protein and vitamin D receptor gene polymorphisms in Iranian patients with chronic periodontitis. Nazemisalman B et al. 2019 Odontology
30166978 Relationship Between Vitamin D Status and Vitamin D Receptor Gene Polymorphisms With Markers of Metabolic Syndrome Among Adults. Karonova T et al. 2018 Frontiers in endocrinology
30220112 Associations among two vitamin D receptor (VDR) gene polymorphisms (ApaI and TaqI) in acne vulgaris: A pilot susceptibility study. Swelam MM et al. 2019 Journal of cosmetic dermatology
30233789 <i>VDR</i> and <i>TNFSF11</i> polymorphisms are associated with osteoporosis in Thai patients. Techapatiphandee M et al. 2018 Biomedical reports
30315926 Haplotypes in vitamin D receptor gene encode risk in diabetic nephropathy. Razi F et al. 2019 Gene
30334169 Hedgehog signaling pathway and vitamin D receptor gene variants as potential risk factors in odontogenic cystic lesions. Magic M et al. 2019 Clinical oral investigations
30334420 Vitamin D receptor gene polymorphisms and prostate cancer. Braczkowski RS et al. 2018 Journal of biological regulators and homeostatic agents
30466214 No Association between Polymorphisms of Vitamin D and Oxytocin Receptor Genes and Autistic Spectrum Disorder in a Sample of Turkish Children. Bozdogan ST et al. 2018 Clinical psychopharmacology and neuroscience
30486759 VDR gene FokI polymorphism as a poor prognostic factor for papillary thyroid cancer. Beysel S et al. 2018 Tumour biology
30584400 Polymorphic Variations in VDR Gene in Saudi Women with and Without Polycystic Ovary Syndrome (PCOS) and Significant Influence of Seven Polymorphic Sites on Anthropometric and Hormonal Parameters. Al Thomali A et al. 2018 Journal of medical biochemistry
30657057 Vitamin D receptor gene polymorphisms and susceptibility for primary osteoarthritis of the knee in a Latin American population. González-Huerta NC et al. 2018 Advances in rheumatology (London, England)
30686249 The Association of Vitamin D Receptor Gene Polymorphism with Lung Cancer Risk: An Update Meta-analysis. Yu ZH et al. 2018 Combinatorial chemistry & high throughput screening
30687119 Association Between Vitamin D Receptor Gene Polymorphisms and Polycystic Ovary Syndrome Risk: A Meta-Analysis. Niu YM et al. 2018 Frontiers in physiology
30699973 Vitamin D Status and Association of <i>VDR</i> Genetic Polymorphism to Risk of Breast Cancer in Ethiopia. Ahmed JH et al. 2019 Nutrients
30730049 The role of vitamin D receptor gene polymorphisms in the pathogenesis of Behçet's disease: A case-control study in Turkish population. Dal NE et al. 2019 Annals of human genetics
30763651 Vitamin D receptor polymorphisms and the susceptibility of Parkinson's disease. Wang X et al. 2019 Neuroscience letters
30764792 Association of vitamin D receptor gene variants with polycystic ovary syndrome: a meta-analysis. Shi XY et al. 2019 BMC medical genetics
30797287 Association between vitamin D receptor gene polymorphisms and pulmonary tuberculosis in a Mexican population. Silva-Ramírez B et al. 2019 The Indian journal of tuberculosis
30822458 A meta-analysis on associations between vitamin D receptor genetic variants and tuberculosis. Wang Y et al. 2019 Microbial pathogenesis
30845908 Relationship of four vitamin D receptor gene polymorphisms with type 1 diabetes mellitus susceptibility in Kuwaiti children. Rasoul MA et al. 2019 BMC pediatrics
30895076 Association of vitamin D receptor gene polymorphisms and periodontitis in a Taiwanese Han population. Ho YP et al. 2017 Journal of dental sciences
30929318 Vitamin D receptor (VDR) TaqI polymorphism, vitamin D and bone mineral density in patients with inflammatory bowel diseases. Szymczak-Tomczak A et al. 2019 Advances in clinical and experimental medicine
30963970 Association of Vitamin D Gene Polymorphisms and Bone Mineral Density in Healthy young Saudi Females. Taha IM et al. 2019 Current molecular medicine
30977086 Strong association between VDR FokI (rs2228570) gene variant and serum vitamin D levels in Turkish Cypriots. Tuncel G et al. 2019 Molecular biology reports
30987490 Associations between vitamin D receptor genetic variants and tuberculosis: a meta-analysis. Xu X et al. 2019 Innate immunity
31006279 The possible role of maternal and placental vitamin D receptor polymorphisms and haplotypes in pathogenesis of preeclampsia. Farajian-Mashhadi F et al. 2019 Clinical and experimental hypertension (New York, N.Y.
31011579 Vitamin D Receptor Gene Polymorphism: An Important Predictor of Arthritis Development. Mukhtar M et al. 2019 BioMed research international
31063999 Genetic Association Study of Restless Legs Syndrome in Chinese Population. Chen J et al. 2019 European neurology
31096931 The VDR gene FokI polymorphism is associated with gestational diabetes mellitus in Turkish women. Apaydın M et al. 2019 BMC medical genetics
31114636 Maternal genetic contribution to pre-pregnancy obesity, gestational weight gain, and gestational diabetes mellitus. Beysel S et al. 2019 Diabetology & metabolic syndrome
31121922 Lower Vitamin D Levels, but Not VDR Polymorphisms, Influence Type 2 Diabetes Mellitus in Brazilian Population Independently of Obesity. Rodrigues KF et al. 2019 Medicina (Kaunas, Lithuania)
31127184 Vitamin D Receptor gene polymorphisms and plasma levels are associated with lumbar disc degeneration. Yang Q et al. 2019 Scientific reports
31190930 Vitamin D receptor rs7975232, rs731236 and rs1544410 single nucleotide polymorphisms, and 25-hydroxyvitamin D levels in Egyptian children with type 1 diabetes mellitus: effect of vitamin D co-therapy. Ahmed AE et al. 2019 Diabetes, metabolic syndrome and obesity
31212049 Association of vitamin D receptor polymorphisms and nephrolithiasis: A meta-analysis. González-Castro TB et al. 2019 Gene

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
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