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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.

rs1801282

Current Build 152

Released October 2, 2018

Organism
Homo sapiens
Position
chr3:12351626 (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
C>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.11119 (27333/245828, GnomAD)
G=0.08278 (10394/125568, TOPMED)
G=0.11014 (13354/121246, ExAC) (+ 5 more)
G=0.1003 (3103/30942, GnomAD)
G=0.070 (352/5008, 1000G)
G=0.164 (734/4480, Estonian)
G=0.119 (460/3854, ALSPAC)
G=0.108 (401/3708, TWINSUK)
Clinical Significance
Reported in ClinVar
Gene : Consequence
PPARG : Missense Variant
Publications
346 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 3 NC_000003.12:g.12351626C>G
GRCh37.p13 chr 3 NC_000003.11:g.12393125C>G
PPARG RefSeqGene NG_011749.1:g.68777C>G
Gene: PPARG, peroxisome proliferator activated receptor gamma (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PPARG transcript variant 5 NM_001330615.1:c. N/A Intron Variant
PPARG transcript variant 6 NM_001354666.1:c. N/A Intron Variant
PPARG transcript variant 7 NM_001354667.1:c. N/A Intron Variant
PPARG transcript variant 9 NM_001354669.1:c. N/A Intron Variant
PPARG transcript variant 10 NM_001354670.1:c. N/A Intron Variant
PPARG transcript variant 4 NM_005037.5:c. N/A Intron Variant
PPARG transcript variant 3 NM_138711.3:c. N/A Intron Variant
PPARG transcript variant 1 NM_138712.3:c. N/A Intron Variant
PPARG transcript variant 2 NM_015869.4:c.34C>G P [CCA] > A [GCA] Coding Sequence Variant
peroxisome proliferator-activated receptor gamma isoform 2 NP_056953.2:p.Pro12Ala P (Pro) > A (Ala) Missense Variant
PPARG transcript variant 8 NM_001354668.1:c.34C>G P [CCA] > A [GCA] Coding Sequence Variant
peroxisome proliferator-activated receptor gamma isoform 4 NP_001341597.1:p.Pro12Ala P (Pro) > A (Ala) Missense Variant
PPARG transcript variant X6 XM_011533844.1:c. N/A Intron Variant
PPARG transcript variant X1 XM_024453604.1:c. N/A Intron Variant
PPARG transcript variant X2 XM_024453605.1:c. N/A Intron Variant
PPARG transcript variant X3 XM_024453606.1:c. N/A Intron Variant
PPARG transcript variant X4 XM_011533842.2:c.34C>G P [CCA] > A [GCA] Coding Sequence Variant
peroxisome proliferator-activated receptor gamma isoform X2 XP_011532144.1:p.Pro12Ala P (Pro) > A (Ala) Missense Variant
PPARG transcript variant X5 XM_011533843.2:c.34C>G P [CCA] > A [GCA] Coding Sequence Variant
peroxisome proliferator-activated receptor gamma isoform X3 XP_011532145.1:p.Pro12Ala P (Pro) > A (Ala) Missense 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: 135465 )
ClinVar Accession Disease Names Clinical Significance
RCV000118044.2 not specified Likely-Benign
RCV000300998.1 Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension Likely-Benign
RCV000336176.1 Familial partial lipodystrophy Likely-Benign
RCV000406618.1 Obesity Likely-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 245828 C=0.88881 G=0.11119
gnomAD - Exomes European Sub 133670 C=0.86889 G=0.13111
gnomAD - Exomes Asian Sub 48002 C=0.9101 G=0.0899
gnomAD - Exomes American Sub 33548 C=0.8793 G=0.1207
gnomAD - Exomes African Sub 15302 C=0.9804 G=0.0196
gnomAD - Exomes Ashkenazi Jewish Sub 9830 C=0.944 G=0.056
gnomAD - Exomes Other Sub 5476 C=0.892 G=0.108
TopMed Global Study-wide 125568 C=0.91722 G=0.08278
ExAC Global Study-wide 121246 C=0.88986 G=0.11014
ExAC Europe Sub 73304 C=0.8741 G=0.1259
ExAC Asian Sub 25102 C=0.9063 G=0.0937
ExAC American Sub 11528 C=0.8721 G=0.1279
ExAC African Sub 10404 C=0.9804 G=0.0196
ExAC Other Sub 908 C=0.90 G=0.10
gnomAD - Genomes Global Study-wide 30942 C=0.8997 G=0.1003
gnomAD - Genomes European Sub 18480 C=0.8614 G=0.1386
gnomAD - Genomes African Sub 8728 C=0.976 G=0.024
gnomAD - Genomes East Asian Sub 1616 C=0.957 G=0.043
gnomAD - Genomes Other Sub 980 C=0.84 G=0.16
gnomAD - Genomes American Sub 836 C=0.90 G=0.10
gnomAD - Genomes Ashkenazi Jewish Sub 302 C=0.92 G=0.08
1000Genomes Global Study-wide 5008 C=0.930 G=0.070
1000Genomes African Sub 1322 C=0.995 G=0.005
1000Genomes East Asian Sub 1008 C=0.974 G=0.026
1000Genomes Europe Sub 1006 C=0.880 G=0.120
1000Genomes South Asian Sub 978 C=0.88 G=0.12
1000Genomes American Sub 694 C=0.88 G=0.12
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.836 G=0.164
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.881 G=0.119
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.892 G=0.108
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 C= G Note
GRCh38.p12 chr 3 NC_000003.12:g.12351626C= NC_000003.12:g.12351626C>G
GRCh37.p13 chr 3 NC_000003.11:g.12393125C= NC_000003.11:g.12393125C>G
PPARG RefSeqGene NG_011749.1:g.68777C= NG_011749.1:g.68777C>G
PPARG transcript variant 2 NM_015869.4:c.34C= NM_015869.4:c.34C>G
PPARG transcript variant 8 NM_001354668.1:c.34C= NM_001354668.1:c.34C>G
PPARG transcript variant X4 XM_011533842.2:c.34C= XM_011533842.2:c.34C>G
PPARG transcript variant X5 XM_011533843.2:c.34C= XM_011533843.2:c.34C>G
peroxisome proliferator-activated receptor gamma isoform 2 NP_056953.2:p.Pro12= NP_056953.2:p.Pro12Ala
peroxisome proliferator-activated receptor gamma isoform 4 NP_001341597.1:p.Pro12= NP_001341597.1:p.Pro12Ala
peroxisome proliferator-activated receptor gamma isoform X2 XP_011532144.1:p.Pro12= XP_011532144.1:p.Pro12Ala
peroxisome proliferator-activated receptor gamma isoform X3 XP_011532145.1:p.Pro12= XP_011532145.1:p.Pro12Ala
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#.

118 SubSNP, 8 Frequency, 4 ClinVar submissions
No Submitter Submission ID Date (Build)
1 HGBASE ss2421521 Nov 14, 2000 (89)
2 PGA-UW-FHCRC ss5587532 Oct 08, 2002 (108)
3 IBARROSO ss12587275 Aug 26, 2003 (117)
4 SSAHASNP ss21914363 Apr 05, 2004 (121)
5 IMCJ-GDT ss22887914 Apr 05, 2004 (121)
6 PARC ss23143926 Sep 20, 2004 (126)
7 PERLEGEN ss24301991 Sep 20, 2004 (123)
8 PGA-UW-FHCRC ss28447437 Sep 20, 2004 (123)
9 ABI ss44380891 Mar 11, 2006 (126)
10 RIVM-TOX ss46533761 Mar 11, 2006 (126)
11 SNP500CANCER ss48296480 Mar 16, 2006 (126)
12 APPLERA_GI ss48423639 Mar 11, 2006 (126)
13 AFFY ss66009632 Nov 29, 2006 (127)
14 AFFY ss66351788 Nov 29, 2006 (127)
15 PERLEGEN ss68853144 May 16, 2007 (127)
16 PHARMGKB_PARC ss69364862 May 16, 2007 (127)
17 PHARMGKB_PARC ss69365041 May 16, 2007 (127)
18 ILLUMINA ss74878796 Dec 06, 2007 (129)
19 AFFY ss76064088 Dec 08, 2007 (130)
20 SI_EXO ss76886233 Dec 06, 2007 (129)
21 KRIBB_YJKIM ss81587013 Dec 14, 2007 (130)
22 CANCER-GENOME ss86343230 Mar 23, 2008 (129)
23 HUMANGENOME_JCVI ss95985793 Feb 03, 2009 (130)
24 BGI ss103902055 Dec 01, 2009 (131)
25 ENSEMBL ss135527614 Dec 01, 2009 (131)
26 ILLUMINA ss160463025 Dec 01, 2009 (131)
27 AFFY ss172373238 Jul 04, 2010 (132)
28 ILLUMINA ss172925497 Jul 04, 2010 (132)
29 PAGE_STUDY ss181341867 Jul 04, 2010 (132)
30 PAGE_STUDY ss181835474 Jul 04, 2010 (132)
31 PAGE_STUDY ss181835892 Jul 04, 2010 (132)
32 PAGE_STUDY ss182258815 Jul 04, 2010 (132)
33 PAGE_STUDY ss182258845 Jul 04, 2010 (132)
34 1000GENOMES ss231711040 Jul 14, 2010 (132)
35 1000GENOMES ss239144608 Jul 15, 2010 (132)
36 OMICIA ss244238258 May 27, 2010 (132)
37 ILLUMINA ss244285129 Jul 04, 2010 (132)
38 BL ss252938256 May 09, 2011 (134)
39 GMI ss277017197 May 04, 2012 (137)
40 PJP ss292934004 May 09, 2011 (134)
41 NHLBI-ESP ss342114366 May 09, 2011 (134)
42 ILLUMINA ss410841189 Sep 17, 2011 (135)
43 ILLUMINA ss480300997 May 04, 2012 (137)
44 ILLUMINA ss480312111 May 04, 2012 (137)
45 ILLUMINA ss481067895 Sep 08, 2015 (146)
46 ILLUMINA ss484948311 May 04, 2012 (137)
47 1000GENOMES ss489865615 May 04, 2012 (137)
48 EXOME_CHIP ss491335705 May 04, 2012 (137)
49 CLINSEQ_SNP ss491829272 May 04, 2012 (137)
50 ILLUMINA ss536094689 Sep 08, 2015 (146)
51 ILLUMINA ss536992457 Sep 08, 2015 (146)
52 TISHKOFF ss556430985 Apr 25, 2013 (138)
53 SSMP ss650097436 Apr 25, 2013 (138)
54 ILLUMINA ss778656867 Aug 21, 2014 (142)
55 ILLUMINA ss780813559 Aug 21, 2014 (142)
56 ILLUMINA ss782920463 Aug 21, 2014 (142)
57 ILLUMINA ss783495615 Aug 21, 2014 (142)
58 ILLUMINA ss783883489 Aug 21, 2014 (142)
59 ILLUMINA ss832175590 Apr 01, 2015 (144)
60 ILLUMINA ss834114824 Aug 21, 2014 (142)
61 OMIM-CURATED-RECORDS ss947846638 Jan 22, 2014 (138)
62 OMIM-CURATED-RECORDS ss947848881 Jan 28, 2014 (138)
63 OMIM-CURATED-RECORDS ss947850201 Feb 04, 2014 (138)
64 OMIM-CURATED-RECORDS ss974293101 Jun 03, 2014 (141)
65 JMKIDD_LAB ss974447037 Aug 21, 2014 (142)
66 EVA-GONL ss978280023 Aug 21, 2014 (142)
67 JMKIDD_LAB ss1067448368 Aug 21, 2014 (142)
68 JMKIDD_LAB ss1070181072 Aug 21, 2014 (142)
69 1000GENOMES ss1302833483 Aug 21, 2014 (142)
70 HAMMER_LAB ss1397329900 Sep 08, 2015 (146)
71 EVA_GENOME_DK ss1579848474 Apr 01, 2015 (144)
72 EVA_FINRISK ss1584025924 Apr 01, 2015 (144)
73 EVA_DECODE ss1587741465 Apr 01, 2015 (144)
74 EVA_UK10K_ALSPAC ss1606431028 Apr 01, 2015 (144)
75 EVA_UK10K_TWINSUK ss1649425061 Apr 01, 2015 (144)
76 EVA_EXAC ss1686873269 Apr 01, 2015 (144)
77 EVA_MGP ss1711007718 Apr 01, 2015 (144)
78 EVA_SVP ss1712554458 Apr 01, 2015 (144)
79 ILLUMINA ss1752436609 Sep 08, 2015 (146)
80 ILLUMINA ss1917763393 Feb 12, 2016 (147)
81 WEILL_CORNELL_DGM ss1921532588 Feb 12, 2016 (147)
82 ILLUMINA ss1946074799 Feb 12, 2016 (147)
83 ILLUMINA ss1958537935 Feb 12, 2016 (147)
84 GENOMED ss1969325361 Jul 19, 2016 (147)
85 JJLAB ss2021319468 Sep 14, 2016 (149)
86 USC_VALOUEV ss2149387220 Dec 20, 2016 (150)
87 HUMAN_LONGEVITY ss2249137180 Dec 20, 2016 (150)
88 TOPMED ss2416180505 Dec 20, 2016 (150)
89 SYSTEMSBIOZJU ss2625160035 Nov 08, 2017 (151)
90 ILLUMINA ss2633912619 Nov 08, 2017 (151)
91 ILLUMINA ss2633912620 Nov 08, 2017 (151)
92 GRF ss2704747940 Nov 08, 2017 (151)
93 GNOMAD ss2733547378 Nov 08, 2017 (151)
94 GNOMAD ss2746947697 Nov 08, 2017 (151)
95 GNOMAD ss2789618248 Nov 08, 2017 (151)
96 AFFY ss2985247271 Nov 08, 2017 (151)
97 AFFY ss2985868338 Nov 08, 2017 (151)
98 SWEGEN ss2991841947 Nov 08, 2017 (151)
99 ILLUMINA ss3022212451 Nov 08, 2017 (151)
100 BIOINF_KMB_FNS_UNIBA ss3024422696 Nov 08, 2017 (151)
101 CSHL ss3344889070 Nov 08, 2017 (151)
102 TOPMED ss3382865436 Nov 08, 2017 (151)
103 ILLUMINA ss3628592064 Oct 11, 2018 (152)
104 ILLUMINA ss3628592065 Oct 11, 2018 (152)
105 ILLUMINA ss3628592066 Oct 11, 2018 (152)
106 ILLUMINA ss3631861132 Oct 11, 2018 (152)
107 ILLUMINA ss3633282347 Oct 11, 2018 (152)
108 ILLUMINA ss3633998836 Oct 11, 2018 (152)
109 ILLUMINA ss3634880715 Oct 11, 2018 (152)
110 ILLUMINA ss3636576888 Oct 11, 2018 (152)
111 ILLUMINA ss3638397631 Oct 11, 2018 (152)
112 ILLUMINA ss3640588018 Oct 11, 2018 (152)
113 ILLUMINA ss3643355925 Oct 11, 2018 (152)
114 ILLUMINA ss3644807350 Oct 11, 2018 (152)
115 OMUKHERJEE_ADBS ss3646282934 Oct 11, 2018 (152)
116 URBANLAB ss3647342604 Oct 11, 2018 (152)
117 ILLUMINA ss3652678577 Oct 11, 2018 (152)
118 ILLUMINA ss3654015795 Oct 11, 2018 (152)
119 1000Genomes NC_000003.11 - 12393125 Oct 11, 2018 (152)
120 The Avon Longitudinal Study of Parents and Children NC_000003.11 - 12393125 Oct 11, 2018 (152)
121 Genetic variation in the Estonian population NC_000003.11 - 12393125 Oct 11, 2018 (152)
122 ExAC NC_000003.11 - 12393125 Oct 11, 2018 (152)
123 gnomAD - Genomes NC_000003.11 - 12393125 Oct 11, 2018 (152)
124 gnomAD - Exomes NC_000003.11 - 12393125 Oct 11, 2018 (152)
125 TopMed NC_000003.12 - 12351626 Oct 11, 2018 (152)
126 UK 10K study - Twins NC_000003.11 - 12393125 Oct 11, 2018 (152)
127 ClinVar RCV000118044.2 Oct 11, 2018 (152)
128 ClinVar RCV000300998.1 Oct 11, 2018 (152)
129 ClinVar RCV000336176.1 Oct 11, 2018 (152)
130 ClinVar RCV000406618.1 Oct 11, 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)
rs17241090 Mar 11, 2006 (126)
rs17749580 Oct 07, 2004 (123)
rs36206375 Oct 25, 2006 (127)
rs56460253 May 23, 2008 (130)
rs57327233 Feb 26, 2009 (130)
Added to this RefSNP Cluster:
Submission ids Observation SPDI Canonical SPDI Source RSIDs
ss66351788, ss76064088, ss160463025, ss172373238, ss244285129, ss252938256, ss277017197, ss292934004, ss410841189, ss480300997, ss491829272, ss1397329900, ss1587741465, ss1712554458, ss3643355925 NC_000003.10:12368124:C= NC_000003.12:12351625:C= (self)
13979456, 7749709, 5480295, 6787755, 130246002, 2078975, 7749709, ss231711040, ss239144608, ss342114366, ss480312111, ss481067895, ss484948311, ss489865615, ss491335705, ss536094689, ss536992457, ss556430985, ss650097436, ss778656867, ss780813559, ss782920463, ss783495615, ss783883489, ss832175590, ss834114824, ss974447037, ss978280023, ss1067448368, ss1070181072, ss1302833483, ss1579848474, ss1584025924, ss1606431028, ss1649425061, ss1686873269, ss1711007718, ss1752436609, ss1917763393, ss1921532588, ss1946074799, ss1958537935, ss1969325361, ss2021319468, ss2149387220, ss2416180505, ss2625160035, ss2633912619, ss2633912620, ss2704747940, ss2733547378, ss2746947697, ss2789618248, ss2985247271, ss2985868338, ss2991841947, ss3022212451, ss3344889070, ss3628592064, ss3628592065, ss3628592066, ss3631861132, ss3633282347, ss3633998836, ss3634880715, ss3636576888, ss3638397631, ss3640588018, ss3644807350, ss3646282934, ss3652678577, ss3654015795 NC_000003.11:12393124:C= NC_000003.12:12351625:C= (self)
244822108, ss244238258, ss947846638, ss947848881, ss947850201, ss974293101, ss2249137180, ss3024422696, ss3382865436, ss3647342604 NC_000003.12:12351625:C= NC_000003.12:12351625:C= (self)
ss21914363 NT_022517.16:12333124:C= NC_000003.12:12351625:C= (self)
ss76886233 NT_022517.17:12333124:C= NC_000003.12:12351625:C= (self)
ss2421521, ss5587532, ss12587275, ss22887914, ss23143926, ss24301991, ss28447437, ss44380891, ss46533761, ss48296480, ss48423639, ss66009632, ss68853144, ss69364862, ss69365041, ss74878796, ss81587013, ss86343230, ss95985793, ss103902055, ss135527614, ss172925497, ss181341867, ss181835474, ss181835892, ss182258815, ss182258845 NT_022517.18:12333124:C= NC_000003.12:12351625:C= (self)
ss66351788, ss76064088, ss160463025, ss172373238, ss244285129, ss252938256, ss277017197, ss292934004, ss410841189, ss480300997, ss491829272, ss1397329900, ss1587741465, ss1712554458, ss3643355925 NC_000003.10:12368124:C>G NC_000003.12:12351625:C>G (self)
13979456, 7749709, 5480295, 6787755, 130246002, 2078975, 7749709, ss231711040, ss239144608, ss342114366, ss480312111, ss481067895, ss484948311, ss489865615, ss491335705, ss536094689, ss536992457, ss556430985, ss650097436, ss778656867, ss780813559, ss782920463, ss783495615, ss783883489, ss832175590, ss834114824, ss974447037, ss978280023, ss1067448368, ss1070181072, ss1302833483, ss1579848474, ss1584025924, ss1606431028, ss1649425061, ss1686873269, ss1711007718, ss1752436609, ss1917763393, ss1921532588, ss1946074799, ss1958537935, ss1969325361, ss2021319468, ss2149387220, ss2416180505, ss2625160035, ss2633912619, ss2633912620, ss2704747940, ss2733547378, ss2746947697, ss2789618248, ss2985247271, ss2985868338, ss2991841947, ss3022212451, ss3344889070, ss3628592064, ss3628592065, ss3628592066, ss3631861132, ss3633282347, ss3633998836, ss3634880715, ss3636576888, ss3638397631, ss3640588018, ss3644807350, ss3646282934, ss3652678577, ss3654015795 NC_000003.11:12393124:C>G NC_000003.12:12351625:C>G (self)
RCV000118044.2, RCV000300998.1, RCV000336176.1, RCV000406618.1, 244822108, ss244238258, ss947846638, ss947848881, ss947850201, ss974293101, ss2249137180, ss3024422696, ss3382865436, ss3647342604 NC_000003.12:12351625:C>G NC_000003.12:12351625:C>G (self)
ss21914363 NT_022517.16:12333124:C>G NC_000003.12:12351625:C>G (self)
ss76886233 NT_022517.17:12333124:C>G NC_000003.12:12351625:C>G (self)
ss2421521, ss5587532, ss12587275, ss22887914, ss23143926, ss24301991, ss28447437, ss44380891, ss46533761, ss48296480, ss48423639, ss66009632, ss68853144, ss69364862, ss69365041, ss74878796, ss81587013, ss86343230, ss95985793, ss103902055, ss135527614, ss172925497, ss181341867, ss181835474, ss181835892, ss182258815, ss182258845 NT_022517.18:12333124:C>G NC_000003.12:12351625:C>G (self)
Help

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

346 citations for rs1801282
PMID Title Author Year Journal
9792554 Association of the Pro12Ala variant in the peroxisome proliferator-activated receptor-gamma2 gene with obesity in two Caucasian populations. Beamer BA et al. 1998 Diabetes
16713673 Variations in the peroxisome proliferator-activated receptor-gamma gene and melanoma risk. Mössner R et al. 2007 Cancer letters
16783862 PPAR-gamma gene polymorphisms and psoriatic arthritis. Butt C et al. 2006 The Journal of rheumatology
17094261 Effect of the peroxisome proliferators-activated receptor (PPAR) gamma 3 gene on BMI in 1,210 school students from Morelos, Mexico. Chen L et al. 2006 Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
17187763 Analysis of PGC-1alpha variants Gly482Ser and Thr612Met concerning their PPARgamma2-coactivation function. Nitz I et al. 2007 Biochemical and biophysical research communications
17213274 Effects of the type 2 diabetes-associated PPARG P12A polymorphism on progression to diabetes and response to troglitazone. Florez JC et al. 2007 The Journal of clinical endocrinology and metabolism
17348446 Nested case-control study of energy regulation candidate gene single nucleotide polymorphisms and breast cancer. Wang Y et al. 2007 Anticancer research
17355643 Frequencies of single nucleotide polymorphisms in genes regulating inflammatory responses in a community-based population. Huang HY et al. 2007 BMC genetics
17570749 Genetic prediction of future type 2 diabetes. Lyssenko V et al. 2005 PLoS medicine
17786212 Heterogeneity in meta-analyses of genome-wide association investigations. Ioannidis JP et al. 2007 PloS one
17825092 Genetic association of glutathione peroxidase-1 with coronary artery calcification in type 2 diabetes: a case control study with multi-slice computed tomography. Nemoto M et al. 2007 Cardiovascular diabetology
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23349771 Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs. Gupta V et al. 2013 PloS one
23386649 Common genetic variants in peroxisome proliferator-activated receptor-γ (PPARG) and type 2 diabetes risk among Women's Health Initiative postmenopausal women. Chan KH et al. 2013 The Journal of clinical endocrinology and metabolism
23462794 Identification of CpG-SNPs associated with type 2 diabetes and differential DNA methylation in human pancreatic islets. Dayeh TA et al. 2013 Diabetologia
23497168 Omega-3 fatty acids, polymorphisms and lipid related cardiovascular disease risk factors in the Inuit population. Rudkowska I et al. 2013 Nutrition & metabolism
23577239 Genetics of obesity and type 2 diabetes in African Americans. McCormack S et al. 2013 Journal of obesity
23633103 Association of Pro12Ala (rs1801282) variant of PPAR gamma with rheumatoid arthritis in a Pakistani population. Jalil SF et al. 2014 Rheumatology international
23874820 Evaluation of 41 candidate gene variants for obesity in the EPIC-Potsdam cohort by multi-locus stepwise regression. Knüppel S et al. 2013 PloS one
23907334 Genetic variants of peroxisome proliferator-activated receptor δ are associated with gastric cancer. Jeon C et al. 2013 Digestive diseases and sciences
23946381 Genetic variants associated with colorectal cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence. Ma X et al. 2014 Gut
24141935 Peroxisome proliferator-activated receptor γ2 Pro12Ala (rs1801282) polymorphism and breast cancer susceptibility: a meta-analysis. Mao Q et al. 2013 Molecular medicine reports
24278702 The complex interplay of genetic and lifestyle risk factors in type 2 diabetes: an overview. Franks PW et al. 2012 Scientifica
24280871 Sleep duration does not mediate or modify association of common genetic variants with type 2 diabetes. Tare A et al. 2014 Diabetologia
24309190 Genetics of new-onset diabetes after transplantation. McCaughan JA et al. 2014 Journal of the American Society of Nephrology
24392269 Gene-Lifestyle Interactions in Obesity. van Vliet-Ostaptchouk JV et al. 2012 Current nutrition reports
24562334 Genetics of oxidative stress in obesity. Rupérez AI et al. 2014 International journal of molecular sciences
24612564 Association of IRS1, CAPN10, and PPARG gene polymorphisms with type 2 diabetes mellitus in the high-risk population of Hyderabad, India. Kommoju UJ et al. 2014 Journal of diabetes
24637646 Cross-sectional and longitudinal replication analyses of genome-wide association loci of type 2 diabetes in Han Chinese. Zhao Q et al. 2014 PloS one
24643342 Effects on metabolic markers are modified by PPARG2 and COX2 polymorphisms in infants randomized to fish oil. Harsløf LB et al. 2014 Genes & nutrition
24653947 Cumulative Effect of Common Genetic Variants Predicts Incident Type 2 Diabetes: A Study of 21,183 Subjects from Three Large Prospective Cohorts. Yang J et al. 2011 Epidemiology (Sunnyvale, Calif.)
24719615 Genetic susceptibility to type 2 diabetes and obesity: follow-up of findings from genome-wide association studies. Basile KJ et al. 2014 International journal of endocrinology
24843374 Association of the PPAR-γ Gene with Altered Glucose Levels and Psychosis Profile in Schizophrenia Patients Exposed to Antipsychotics. Liu YR et al. 2014 Psychiatry investigation
24843659 Insights into the genetic basis of type 2 diabetes. Kato N et al. 2013 Journal of diabetes investigation
24845081 Gene-lifestyle interaction and type 2 diabetes: the EPIC interact case-cohort study. Langenberg C et al. 2014 PLoS medicine
24864266 Genetics of type 2 diabetes: insights into the pathogenesis and its clinical application. Sun X et al. 2014 BioMed research international
24879436 Replication of 6 obesity genes in a meta-analysis of genome-wide association studies from diverse ancestries. Tan LJ et al. 2014 PloS one
24889212 Systematic review: interactions between aspirin, and other nonsteroidal anti-inflammatory drugs, and polymorphisms in relation to colorectal cancer. Andersen V et al. 2014 Alimentary pharmacology & therapeutics
24926958 Evaluation of common type 2 diabetes risk variants in a South Asian population of Sri Lankan descent. Hassanali N et al. 2014 PloS one
24929251 Gene-carbohydrate and gene-fiber interactions and type 2 diabetes in diverse populations from the National Health and Nutrition Examination Surveys (NHANES) as part of the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) study. Villegas R et al. 2014 BMC genetics
24935819 Exploring genetic variants predisposing to diabetes mellitus and their association with indicators of socioeconomic status. Schmidt B et al. 2014 BMC public health
24971461 Polymorphisms in the inflammatory pathway genes TLR2, TLR4, TLR9, LY96, NFKBIA, NFKB1, TNFA, TNFRSF1A, IL6R, IL10, IL23R, PTPN22, and PPARG are associated with susceptibility of inflammatory bowel disease in a Danish cohort. Bank S et al. 2014 PloS one
24982668 Estimating the predictive ability of genetic risk models in simulated data based on published results from genome-wide association studies. Kundu S et al. 2014 Frontiers in genetics
25043640 Polymorphisms of peroxisome proliferator-activated receptors and survival of lung cancer and upper aero-digestive tract cancers. Yang Y et al. 2014 Lung cancer (Amsterdam, Netherlands)
25063576 Development of ARMS-PCR assay for genotyping of Pro12Ala SNP of PPARG gene: a cost effective way for case-control studies of type 2 diabetes in developing countries. Islam M et al. 2014 Molecular biology reports
25072612 PPARγ2 Pro12Ala polymorphism is associated with sustained virological response in HIV/HCV-coinfected patients under HCV therapy. Fernández-Rodríguez A et al. 2014 Journal of acquired immune deficiency syndromes (1999)
25145545 Does genetic heterogeneity account for the divergent risk of type 2 diabetes in South Asian and white European populations? Sohani ZN et al. 2014 Diabetologia
25182148 The Pro12Ala polymorphism in the peroxisome proliferator-activated receptor gamma (PPARG) gene in relation to obesity and metabolic phenotypes in a Taiwanese population. Hsiao TJ et al. 2015 Endocrine
25224558 Association of variants in genes related to the immune response and obesity with BPH in CLUE II. Lopez DS et al. 2014 Prostate cancer and prostatic diseases
25260659 Omental adipose tissue gene expression, gene variants, branched-chain amino acids, and their relationship with metabolic syndrome and insulin resistance in humans. Serralde-Zúñiga AE et al. 2014 Genes & nutrition
25262148 The association between lipid metabolism gene polymorphisms and nephropathy in type 2 diabetes: a meta-analysis. Li T et al. 2015 International urology and nephrology
25274455 The gene polymorphisms of UCP1 but not PPAR γ and TCF7L2 are associated with diabetic retinopathy in Chinese type 2 diabetes mellitus cases. Zhang Y et al. 2015 Acta ophthalmologica
25406242 Pro12Ala polymorphism of the PPARγ2 gene interacts with a mediterranean diet to prevent telomere shortening in the PREDIMED-NAVARRA randomized trial. García-Calzón S et al. 2015 Circulation. Cardiovascular genetics
25430627 A genetic risk tool for obesity predisposition assessment and personalized nutrition implementation based on macronutrient intake. Goni L et al. 2015 Genes & nutrition
25487307 The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy. Hosseini SM et al. 2015 Human genetics
25488145 Dietary inflammatory index and inflammatory gene interactions in relation to colorectal cancer risk in the Bellvitge colorectal cancer case-control study. Zamora-Ros R et al. 2015 Genes & nutrition
25516658 Case-control study of diabetes-related genetic variants and pancreatic cancer risk in Japan. Kuruma S et al. 2014 World journal of gastroenterology
25685286 Adiponectin: Probe of the molecular paradigm associating diabetes and obesity. Ghoshal K et al. 2015 World journal of diabetes
25770052 Lack of genetic associations between PPAR-γ gene rs1801282 polymorphism and Alzheimer's disease in general population: a meta-analysis. Wu Y et al. 2015 Gene
25774817 Genetics of type 2 diabetes-pitfalls and possibilities. Prasad RB et al. 2015 Genes
25832497 Association between Peroxisome Proliferator-activated Receptor Gamma Gene Polymorphisms and Atherosclerotic Diseases: A Meta-analysis of Case-control Studies. Wang P et al. 2015 Journal of atherosclerosis and thrombosis
25839936 Diabetes susceptibility in Mayas: Evidence for the involvement of polymorphisms in HHEX, HNF4α, KCNJ11, PPARγ, CDKN2A/2B, SLC30A8, CDC123/CAMK1D, TCF7L2, ABCA1 and SLC16A11 genes. Lara-Riegos JC et al. 2015 Gene
25887915 Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan. Ilyas M et al. 2015 BMC genomics
25923461 IGF2, LEPR, POMC, PPARG, and PPARGC1 gene variants are associated with obesity-related risk phenotypes in Brazilian children and adolescents. Queiroz EM et al. 2015 Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas
25986483 A candidate gene study reveals association between a variant of the Peroxisome Proliferator-Activated Receptor Gamma (PPAR-γ) gene and systemic sclerosis. Marangoni RG et al. 2015 Arthritis research & therapy
26042206 Gene-gene and gene-environment interactions in the etiology of type 2 diabetes mellitus in the population of Hyderabad, India. Uma Jyothi K et al. 2015 Meta gene
26240488 Utilizing Genetic Predisposition Score in Predicting Risk of Type 2 Diabetes Mellitus Incidence: A Community-based Cohort Study on Middle-aged Koreans. Park HY et al. 2015 Journal of Korean medical science
26243686 Implications of critical PPARγ2, ADIPOQ and FTO gene polymorphisms in type 2 diabetes and obesity-mediated susceptibility to type 2 diabetes in an Indian population. Phani NM et al. 2016 Molecular genetics and genomics
26273662 Association of the Genetic Polymorphisms in Transcription Factor 7-Like 2 and Peroxisome Proliferator-Activated Receptors- γ 2 with Type 2 Diabetes Mellitus and is Interaction with Obesity Status in Emirati Population. Al-Safar H et al. 2015 Journal of diabetes research
26331316 Prevalence of the rs1801282 single nucleotide polymorphism of the PPARG gene in patients with metabolic syndrome. Rocha RM et al. 2015 Archives of endocrinology and metabolism
26621708 Human-specific derived alleles of CD33 and other genes protect against postreproductive cognitive decline. Schwarz F et al. 2016 Proceedings of the National Academy of Sciences of the United States of America
26648684 Update on genetics and diabetic retinopathy. Hampton BM et al. 2015 Clinical ophthalmology (Auckland, N.Z.)
26789123 A HuGE Review and Meta-Analyses of Genetic Associations in New Onset Diabetes after Kidney Transplantation. Benson KA et al. 2016 PloS one
26833210 Evaluation of pleiotropic effects among common genetic loci identified for cardio-metabolic traits in a Korean population. Kim YK et al. 2016 Cardiovascular diabetology
26881045 Interplay between Superoxide Dismutase, Glutathione Peroxidase, and Peroxisome Proliferator Activated Receptor Gamma Polymorphisms on the Risk of End-Stage Renal Disease among Han Chinese Patients. Chao CT et al. 2016 Oxidative medicine and cellular longevity
26930408 Association between Maternal Fish Consumption and Gestational Weight Gain: Influence of Molecular Genetic Predisposition to Obesity. Larsen SC et al. 2016 PloS one
26933222 Alzheimer's disease CD33 rs3865444 variant does not contribute to cognitive performance. Liu G et al. 2016 Proceedings of the National Academy of Sciences of the United States of America
26937418 Candidate gene analysis supports a role for polymorphisms at TCF7L2 as risk factors for type 2 diabetes in Sudan. Ibrahim AT et al. 2015 Journal of diabetes and metabolic disorders
26949382 Polymorphisms of the PPAR-γ (rs1801282) and Its Coactivator (rs8192673) Have a Minor Effect on Markers of Carotid Atherosclerosis in Patients with Type 2 Diabetes Mellitus. Pleskovič A et al. 2016 PPAR research
26956846 The PPARγ2 P12A polymorphism is not associated with all-cause mortality in patients with type 2 diabetes mellitus. Pacilli A et al. 2016 Endocrine
26964836 Recent progress in genetic and epigenetic research on type 2 diabetes. Kwak SH et al. 2016 Experimental & molecular medicine
26965314 Gene polymorphisms associated with non-alcoholic fatty liver disease and coronary artery disease: a concise review. Li XL et al. 2016 Lipids in health and disease
26983698 Joint effects of diabetic-related genomic loci on the therapeutic efficacy of oral anti-diabetic drugs in Chinese type 2 diabetes patients. Chen M et al. 2016 Scientific reports
26999420 Genetic polymorphisms associated with overweight and obesity in uncontrolled Type 2 diabetes mellitus. Kasim NB et al. 2016 Biomarkers in medicine
27042264 Genetics of cardiovascular and renal complications in diabetes. Ma RC et al. 2016 Journal of diabetes investigation
27051588 Analysis of single nucleotide polymorphisms implicate mTOR signalling in the development of new-onset diabetes after transplantation. Chand S et al. 2016 BBA clinical
27053236 Evaluation of type 2 diabetes genetic risk variants in Chinese adults: findings from 93,000 individuals from the China Kadoorie Biobank. Gan W et al. 2016 Diabetologia
27089360 Nutritional Genomics and the Mediterranean Diet's Effects on Human Cardiovascular Health. Fitó M et al. 2016 Nutrients
27102200 Alcohol-related breast cancer in postmenopausal women - effect of CYP19A1, PPARG and PPARGC1A polymorphisms on female sex-hormone levels and interaction with alcohol consumption and NSAID usage in a nested case-control study and a randomised controlled trial. Kopp TI et al. 2016 BMC cancer
27103840 Pharmacogenetics in type 2 diabetes: influence on response to oral hypoglycemic agents. Dawed AY et al. 2016 Pharmacogenomics and personalized medicine
27159875 Sex and Gender Differences in Risk, Pathophysiology and Complications of Type 2 Diabetes Mellitus. Kautzky-Willer A et al. 2016 Endocrine reviews
27207512 Variants in Genes Controlling Oxidative Metabolism Contribute to Lower Hepatic ATP Independent of Liver Fat Content in Type 1 Diabetes. Gancheva S et al. 2016 Diabetes
27211558 Type 2 Diabetes, Diabetes Genetic Score and Risk of Decreased Renal Function and Albuminuria: A Mendelian Randomization Study. Xu M et al. 2016 EBioMedicine
27217270 Pharmacogenetic Associations of Antipsychotic Drug-Related Weight Gain: A Systematic Review and Meta-analysis. Zhang JP et al. 2016 Schizophrenia bulletin
27246401 Genetic Background, Adipocytokines, and Metabolic Disorders in Postmenopausal Overweight and Obese Women. Grygiel-Górniak B et al. 2016 Biochemical genetics
27347941 Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes. Costa V et al. 2016 International journal of molecular sciences
27383215 Type 2 Diabetes Risk Allele Loci in the Qatari Population. O'Beirne SL et al. 2016 PloS one
27417569 Systematic review: genetic biomarkers associated with anti-TNF treatment response in inflammatory bowel diseases. Bek S et al. 2016 Alimentary pharmacology & therapeutics
27468700 Genetic variants associated with gestational diabetes mellitus: a meta-analysis and subgroup analysis. Wu L et al. 2016 Scientific reports
27483259 Is the Mouse a Good Model of Human PPARγ-Related Metabolic Diseases? Pap A et al. 2016 International journal of molecular sciences
27515755 Study of seven single-nucleotide polymorphisms identified in East Asians for association with obesity in a Taiwanese population. Huang WH et al. 2016 BMJ open
27551309 Several type 2 diabetes-associated variants in genes annotated to WNT signaling interact with dietary fiber in relation to incidence of type 2 diabetes. Hindy G et al. 2016 Genes & nutrition
27560839 Polymorphisms FTO rs9939609, PPARG rs1801282 and ADIPOQ rs4632532 and rs182052 but not lifestyle are associated with obesity related-traits in Mexican children. Muñoz-Yáñez C et al. 2016 Genetics and molecular biology
27601774 Genetic variants influencing effectiveness of exercise training programmes in obesity - an overview of human studies. Leońska-Duniec A et al. 2016 Biology of sport
27730450 Candidate gene studies of diabetic retinopathy in human. Priščáková P et al. 2016 Molecular biology reports
27806373 The Genetic Predisposition Score of Seven Obesity-Related Single Nucleotide Polymorphisms Is Associated with Better Metabolic Outcomes after Roux-en-Y Gastric Bypass. Nicoletti CF et al. 2016 Journal of nutrigenetics and nutrigenomics
27883295 Identification of novel SNPs associated with risk and prognosis in patients with castration-resistant prostate cancer. Sissung TM et al. 2016 Pharmacogenomics
27920511 Relationships between <i>FTO</i> rs9939609, <i>MC4R</i> rs17782313, and <i>PPARγ</i> rs1801282 polymorphisms and the occurrence of selected metabolic and hormonal disorders in middle-aged and elderly men - a preliminary study. Rotter I et al. 2016 Clinical interventions in aging
28090739 Obesity-related genetic polymorphisms and adiposity indices in a young Italian population. Bordoni L et al. 2017 IUBMB life
28133617 Molecular Analysis of a Genetic Variants Panel Related to Nutrients and Metabolism: Association with Susceptibility to Gestational Diabetes and Cardiometabolic Risk in Affected Women. Franzago M et al. 2017 Journal of diabetes research
28283271 Multiple chemical sensitivity: Genotypic characterization, nutritional status and quality of life in 52 patients. Loria-Kohen V et al. 2017 Medicina clinica
28290785 [Genetic Risk Factors of Macrovascular Complications in Patients With Type 2 Diabetes]. Bystrova AA et al. 2017 Kardiologiia
28418876 PPARGC1A rs3736265 G&gt;A polymorphism is associated with decreased risk of type 2 diabetes mellitus and fasting plasma glucose level. Zhu L et al. 2017 Oncotarget
28578327 Genetic Predictors of ≥5% Weight Loss by Multidisciplinary Advice to Severely Obese Subjects. Aller EEJG et al. 2017 Journal of nutrigenetics and nutrigenomics
28699988 Type 2 diabetes-associated genetic variants of FTO, LEPR, PPARg, and TCF7L2 in gestational diabetes in a Brazilian population. Anghebem-Oliveira MI et al. 2017 Archives of endocrinology and metabolism
28738793 Association between 28 single nucleotide polymorphisms and type 2 diabetes mellitus in the Kazakh population: a case-control study. Sikhayeva N et al. 2017 BMC medical genetics
28821857 CDKAL1 rs7756992 is associated with diabetic retinopathy in a Chinese population with type 2 diabetes. Peng D et al. 2017 Scientific reports
28827564 The profile of selected single nucleotide polymorphisms in patients with hypertension and heart failure with preserved and mid-range ejection fraction. Bielecka-Dabrowa A et al. 2017 Scientific reports
28827732 Genetic predisposition to lung cancer: comprehensive literature integration, meta-analysis, and multiple evidence assessment of candidate-gene association studies. Wang J et al. 2017 Scientific reports
29055064 Clinical relevance of peroxisome proliferator-activated receptor-γ gene polymorphisms with sepsis. Liu Y et al. 2018 Journal of clinical laboratory analysis
29200867 The relationship between <i>IGF2BP2</i> and <i>PPARG</i> polymorphisms and susceptibility to esophageal squamous-cell carcinomas in the eastern Chinese Han population. Qiu H et al. 2017 OncoTargets and therapy
29246001 Association of <i>PPARG</i> rs 1801282 C&gt;G polymorphism with risk of colorectal cancer: from a case-control study to a meta-analysis. Jiang J et al. 2017 Oncotarget
29256014 Genetic variation in TNFα, PPARγ, and IRS-1 genes, and their association with breast-cancer survival in the HEAL cohort. Duggan C et al. 2018 Breast cancer research and treatment
29273888 Identification of pleiotropic genetic variants affecting osteoporosis risk in a Korean elderly cohort. Hong EP et al. 2019 Journal of bone and mineral metabolism
29303622 Genotype-based recall to study metabolic effects of genetic variation: a pilot study of PPARG Pro12Ala carriers. Kamble PG et al. 2017 Upsala journal of medical sciences
29315078 Associations between the components of metabolic syndrome and the polymorphisms in the peroxisome proliferator-activated receptor gamma (<i>PPAR-γ</i>), the fat mass and obesity-associated (<i>FTO</i>), and the melanocortin-4 receptor (<i>MC4R</i>) genes. Szkup M et al. 2018 Aging
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29369552 [Association of variable rs1801282 locus of PPARG2 gene with diabetic nephropathy]. Avzaletdinova DS et al. 2016 Genetika
29402778 Interaction of Vitamin E Intake and Pro12Ala Polymorphism of PPARG with Adiponectin Levels. Campos-Perez W et al. 2017 Journal of nutrigenetics and nutrigenomics
29494521 Influence of Single-Nucleotide Polymorphisms in PPAR-δ, PPAR-γ, and PRKAA2 on the Changes in Anthropometric Indices and Blood Measurements through Exercise-Centered Lifestyle Intervention in Japanese Middle-Aged Men. Nishida Y et al. 2018 International journal of molecular sciences
29496354 Expression of the gene coading for PGC-1α in peripheral blood leukocytes and related gene variants in patients with Parkinson's disease. Yang XD et al. 2018 Parkinsonism & related disorders
29610599 Is the rs1801282 (G/C) Polymorphism of <i>PPAR - Gamma</i> Gene Associated with T2DM in Iraqi People? Al-Naemi AH et al. 2018 Open access Macedonian journal of medical sciences
29665413 Genetic risk factors for post-transplantation diabetes mellitus in Chinese Han renal allograft recipients treated with tacrolimus. Zhang X et al. 2018 Transplant immunology
29679223 Association between LEPR, FTO, MC4R, and PPARG-2 polymorphisms with obesity traits and metabolic phenotypes in school-aged children. Almeida SM et al. 2018 Endocrine
29703528 Replication of a Gene-Diet Interaction at CD36, NOS3 and PPARG in Response to Omega-3 Fatty Acid Supplements on Blood Lipids: A Double-Blind Randomized Controlled Trial. Zheng JS et al. 2018 EBioMedicine
29762540 The Role of Peroxisome Proliferator-Activated Receptors and Their Transcriptional Coactivators Gene Variations in Human Trainability: A Systematic Review. Petr M et al. 2018 International journal of molecular sciences
29795275 Phenotype and genotype predictors of BMI variability among European adults. Goni L et al. 2018 Nutrition & diabetes
29800730 The ADRA2A rs553668 variant is associated with type 2 diabetes and five variants were associated at nominal significance levels in a population-based case-control study from Mexico City. Totomoch-Serra A et al. 2018 Gene
29885389 Geographic diversity in genotype frequencies and meta-analysis of the association between rs1801282 polymorphisms and gestational diabetes mellitus. Lin PC et al. 2018 Diabetes research and clinical practice
29970681 Peroxisome proliferators-activated receptor gamma polymorphisms and colorectal cancer risk. Liang X et al. 2018 Journal of cancer research and therapeutics
30026785 <i>PPARG2</i> Pro12Ala polymorphism influences body composition changes in severely obese patients consuming extra virgin olive oil: a randomized clinical trial. Rodrigues APS et al. 2018 Nutrition & metabolism
30041843 Genetic susceptibility to pre diabetes mellitus and related association with obesity and physical fitness components in Mexican-Mestizos. Costa-Urrutia P et al. 2018 Primary care diabetes
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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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