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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

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.

rs2414739

Current Build 154

Released April 21, 2020

Organism
Homo sapiens
Position
chr15:61701935 (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
G>A
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.268722 (43813/163042, ALFA Project)
G=0.321714 (40397/125568, TOPMED)
G=0.33622 (26228/78008, PAGE_STUDY) (+ 16 more)
G=0.33463 (10490/31348, GnomAD)
G=0.3209 (1607/5008, 1000G)
G=0.3408 (1527/4480, Estonian)
G=0.2548 (982/3854, ALSPAC)
G=0.2508 (930/3708, TWINSUK)
G=0.1853 (543/2930, KOREAN)
G=0.2879 (600/2084, HGDP_Stanford)
G=0.3076 (582/1892, HapMap)
G=0.1900 (348/1832, Korea1K)
G=0.257 (256/998, GoNL)
G=0.235 (141/600, NorthernSweden)
G=0.216 (110/510, SGDP_PRJ)
G=0.269 (58/216, Qatari)
G=0.210 (45/214, Vietnamese)
G=0.23 (11/48, Siberian)
G=0.28 (11/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
LOC107984782 : Intron Variant
Publications
6 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 15 NC_000015.10:g.61701935G>A
GRCh37.p13 chr 15 NC_000015.9:g.61994134G>A
Gene: LOC107984782, uncharacterized LOC107984782 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
LOC107984782 transcript variant X1 XR_001751569.1:n. N/A Intron Variant
LOC107984782 transcript variant X2 XR_001751570.1:n. N/A Genic Upstream Transcript 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.

Not Reported in ClinVar

ALFA Allele Frequency (New)
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 324984 G=0.269583 A=0.730417
European Sub 286816 G=0.265923 A=0.734077
African Sub 8380 G=0.4675 A=0.5325
African Others Sub 318 G=0.538 A=0.462
African American Sub 8062 G=0.4648 A=0.5352
Asian Sub 3940 G=0.1921 A=0.8079
East Asian Sub 3194 G=0.1863 A=0.8137
Other Asian Sub 746 G=0.217 A=0.783
Latin American 1 Sub 1134 G=0.3086 A=0.6914
Latin American 2 Sub 7220 G=0.2127 A=0.7873
South Asian Sub 5222 G=0.3097 A=0.6903
Other Sub 12272 G=0.25758 A=0.74242


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
ALFA Total Global 163042 G=0.268722 A=0.731278
ALFA European Sub 142526 G=0.265418 A=0.734582
ALFA Other Sub 5970 G=0.2590 A=0.7410
ALFA Latin American 2 Sub 5436 G=0.2064 A=0.7936
ALFA South Asian Sub 4898 G=0.3101 A=0.6899
ALFA African Sub 3354 G=0.4693 A=0.5307
ALFA Latin American 1 Sub 562 G=0.313 A=0.687
ALFA Asian Sub 296 G=0.159 A=0.841
TopMed Global Study-wide 125568 G=0.321714 A=0.678286
The PAGE Study Global Study-wide 78008 G=0.33622 A=0.66378
The PAGE Study AfricanAmerican Sub 32218 G=0.46977 A=0.53023
The PAGE Study Mexican Sub 10722 G=0.20211 A=0.79789
The PAGE Study Asian Sub 8246 G=0.2338 A=0.7662
The PAGE Study PuertoRican Sub 7860 G=0.2912 A=0.7088
The PAGE Study NativeHawaiian Sub 4494 G=0.1297 A=0.8703
The PAGE Study Cuban Sub 4198 G=0.2668 A=0.7332
The PAGE Study Dominican Sub 3782 G=0.3461 A=0.6539
The PAGE Study CentralAmerican Sub 2428 G=0.2549 A=0.7451
The PAGE Study SouthAmerican Sub 1960 G=0.2439 A=0.7561
The PAGE Study NativeAmerican Sub 1252 G=0.2780 A=0.7220
The PAGE Study SouthAsian Sub 848 G=0.297 A=0.703
gnomAD - Genomes Global Study-wide 31348 G=0.33463 A=0.66537
gnomAD - Genomes European Sub 18870 G=0.29089 A=0.70911
gnomAD - Genomes African Sub 8702 G=0.4794 A=0.5206
gnomAD - Genomes East Asian Sub 1554 G=0.1647 A=0.8353
gnomAD - Genomes Other Sub 1086 G=0.2808 A=0.7192
gnomAD - Genomes American Sub 848 G=0.217 A=0.783
gnomAD - Genomes Ashkenazi Jewish Sub 288 G=0.292 A=0.708
1000Genomes Global Study-wide 5008 G=0.3209 A=0.6791
1000Genomes African Sub 1322 G=0.5182 A=0.4818
1000Genomes East Asian Sub 1008 G=0.1935 A=0.8065
1000Genomes Europe Sub 1006 G=0.2793 A=0.7207
1000Genomes South Asian Sub 978 G=0.301 A=0.699
1000Genomes American Sub 694 G=0.219 A=0.781
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.3408 A=0.6592
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.2548 A=0.7452
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.2508 A=0.7492
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.1853 A=0.8147
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.2879 A=0.7121
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.223 A=0.777
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.312 A=0.688
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.251 A=0.749
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.300 A=0.700
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.483 A=0.517
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.204 A=0.796
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.29 A=0.71
HapMap Global Study-wide 1892 G=0.3076 A=0.6924
HapMap American Sub 770 G=0.286 A=0.714
HapMap African Sub 692 G=0.379 A=0.621
HapMap Asian Sub 254 G=0.209 A=0.791
HapMap Europe Sub 176 G=0.267 A=0.733
Korean Genome Project KOREAN Study-wide 1832 G=0.1900 A=0.8100
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.257 A=0.743
Northern Sweden ACPOP Study-wide 600 G=0.235 A=0.765
SGDP_PRJ Global Study-wide 510 G=0.216 A=0.784
Qatari Global Study-wide 216 G=0.269 A=0.731
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.210 A=0.790
Siberian Global Study-wide 48 G=0.23 A=0.77
The Danish reference pan genome Danish Study-wide 40 G=0.28 A=0.72
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 G= A
GRCh38.p12 chr 15 NC_000015.10:g.61701935= NC_000015.10:g.61701935G>A
GRCh37.p13 chr 15 NC_000015.9:g.61994134= NC_000015.9:g.61994134G>A
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#.

125 SubSNP, 19 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss3381940 Sep 28, 2001 (100)
2 SSAHASNP ss21246596 Apr 05, 2004 (121)
3 PERLEGEN ss23812432 Sep 20, 2004 (123)
4 ABI ss43770986 Mar 15, 2006 (126)
5 AFFY ss65996768 Nov 30, 2006 (127)
6 ILLUMINA ss66743331 Nov 30, 2006 (127)
7 ILLUMINA ss67252902 Nov 30, 2006 (127)
8 ILLUMINA ss67650838 Nov 30, 2006 (127)
9 PERLEGEN ss69178862 May 17, 2007 (127)
10 ILLUMINA ss70731246 May 23, 2008 (130)
11 ILLUMINA ss71300757 May 17, 2007 (127)
12 ILLUMINA ss75727268 Dec 07, 2007 (129)
13 ILLUMINA ss79134174 Dec 14, 2007 (130)
14 KRIBB_YJKIM ss84047092 Dec 14, 2007 (130)
15 HGSV ss84827229 Dec 14, 2007 (130)
16 BCMHGSC_JDW ss90183034 Mar 24, 2008 (129)
17 HUMANGENOME_JCVI ss96764673 Feb 03, 2009 (130)
18 BGI ss106435113 Feb 03, 2009 (130)
19 1000GENOMES ss108879053 Jan 23, 2009 (130)
20 1000GENOMES ss114284275 Jan 25, 2009 (130)
21 ILLUMINA-UK ss118256259 Feb 14, 2009 (130)
22 ILLUMINA ss122030245 Dec 01, 2009 (131)
23 ENSEMBL ss136384573 Dec 01, 2009 (131)
24 ENSEMBL ss136881876 Dec 01, 2009 (131)
25 ILLUMINA ss153910805 Dec 01, 2009 (131)
26 GMI ss156632797 Dec 01, 2009 (131)
27 ILLUMINA ss159388636 Dec 01, 2009 (131)
28 ILLUMINA ss160545537 Dec 01, 2009 (131)
29 COMPLETE_GENOMICS ss168163921 Jul 04, 2010 (132)
30 COMPLETE_GENOMICS ss169693806 Jul 04, 2010 (132)
31 COMPLETE_GENOMICS ss171216647 Jul 04, 2010 (132)
32 ILLUMINA ss171248276 Jul 04, 2010 (132)
33 ILLUMINA ss173334539 Jul 04, 2010 (132)
34 BUSHMAN ss200935640 Jul 04, 2010 (132)
35 BCM-HGSC-SUB ss207209511 Jul 04, 2010 (132)
36 1000GENOMES ss226932591 Jul 14, 2010 (132)
37 1000GENOMES ss236806897 Jul 15, 2010 (132)
38 1000GENOMES ss243189113 Jul 15, 2010 (132)
39 BL ss255043545 May 09, 2011 (134)
40 GMI ss282286589 May 04, 2012 (137)
41 GMI ss286967485 Apr 25, 2013 (138)
42 PJP ss291735851 May 09, 2011 (134)
43 ILLUMINA ss480562555 May 04, 2012 (137)
44 ILLUMINA ss480576946 May 04, 2012 (137)
45 ILLUMINA ss481396415 Sep 08, 2015 (146)
46 ILLUMINA ss485076865 May 04, 2012 (137)
47 ILLUMINA ss537088444 Sep 08, 2015 (146)
48 TISHKOFF ss564526497 Apr 25, 2013 (138)
49 SSMP ss660257447 Apr 25, 2013 (138)
50 ILLUMINA ss778495485 Sep 08, 2015 (146)
51 ILLUMINA ss782984720 Sep 08, 2015 (146)
52 ILLUMINA ss783945662 Sep 08, 2015 (146)
53 ILLUMINA ss825464692 Apr 01, 2015 (144)
54 ILLUMINA ss832241372 Sep 08, 2015 (146)
55 ILLUMINA ss832900393 Jul 13, 2019 (153)
56 ILLUMINA ss833951537 Sep 08, 2015 (146)
57 EVA-GONL ss991863599 Aug 21, 2014 (142)
58 JMKIDD_LAB ss1080186503 Aug 21, 2014 (142)
59 1000GENOMES ss1353766503 Aug 21, 2014 (142)
60 DDI ss1427649981 Apr 01, 2015 (144)
61 EVA_GENOME_DK ss1577661747 Apr 01, 2015 (144)
62 EVA_UK10K_ALSPAC ss1633160246 Apr 01, 2015 (144)
63 EVA_UK10K_TWINSUK ss1676154279 Apr 01, 2015 (144)
64 EVA_DECODE ss1695885015 Apr 01, 2015 (144)
65 EVA_SVP ss1713495993 Apr 01, 2015 (144)
66 ILLUMINA ss1752166759 Sep 08, 2015 (146)
67 HAMMER_LAB ss1808238455 Sep 08, 2015 (146)
68 WEILL_CORNELL_DGM ss1935270898 Feb 12, 2016 (147)
69 ILLUMINA ss1946395755 Feb 12, 2016 (147)
70 ILLUMINA ss1959618480 Feb 12, 2016 (147)
71 GENOMED ss1968127408 Jul 19, 2016 (147)
72 JJLAB ss2028415348 Sep 14, 2016 (149)
73 ILLUMINA ss2095059515 Dec 20, 2016 (150)
74 USC_VALOUEV ss2156820101 Dec 20, 2016 (150)
75 HUMAN_LONGEVITY ss2207408648 Dec 20, 2016 (150)
76 TOPMED ss2371834099 Dec 20, 2016 (150)
77 SYSTEMSBIOZJU ss2628703241 Nov 08, 2017 (151)
78 ILLUMINA ss2633239664 Nov 08, 2017 (151)
79 GRF ss2701294350 Nov 08, 2017 (151)
80 ILLUMINA ss2710818441 Nov 08, 2017 (151)
81 GNOMAD ss2935758526 Nov 08, 2017 (151)
82 SWEGEN ss3013403497 Nov 08, 2017 (151)
83 ILLUMINA ss3021640129 Nov 08, 2017 (151)
84 BIOINF_KMB_FNS_UNIBA ss3028032244 Nov 08, 2017 (151)
85 TOPMED ss3229603873 Nov 08, 2017 (151)
86 CSHL ss3351150478 Nov 08, 2017 (151)
87 ILLUMINA ss3625674876 Oct 12, 2018 (152)
88 ILLUMINA ss3627378938 Oct 12, 2018 (152)
89 ILLUMINA ss3631231758 Oct 12, 2018 (152)
90 ILLUMINA ss3633100140 Oct 12, 2018 (152)
91 ILLUMINA ss3633804843 Oct 12, 2018 (152)
92 ILLUMINA ss3634610324 Oct 12, 2018 (152)
93 ILLUMINA ss3635493695 Oct 12, 2018 (152)
94 ILLUMINA ss3636300394 Oct 12, 2018 (152)
95 ILLUMINA ss3637244982 Oct 12, 2018 (152)
96 ILLUMINA ss3638090055 Oct 12, 2018 (152)
97 ILLUMINA ss3639058159 Oct 12, 2018 (152)
98 ILLUMINA ss3639534428 Oct 12, 2018 (152)
99 ILLUMINA ss3640317645 Oct 12, 2018 (152)
100 ILLUMINA ss3643073971 Oct 12, 2018 (152)
101 ILLUMINA ss3644648856 Oct 12, 2018 (152)
102 URBANLAB ss3650371450 Oct 12, 2018 (152)
103 ILLUMINA ss3652041259 Oct 12, 2018 (152)
104 EGCUT_WGS ss3680549946 Jul 13, 2019 (153)
105 EVA_DECODE ss3698039558 Jul 13, 2019 (153)
106 ILLUMINA ss3725506115 Jul 13, 2019 (153)
107 ACPOP ss3740989463 Jul 13, 2019 (153)
108 ILLUMINA ss3744132234 Jul 13, 2019 (153)
109 ILLUMINA ss3744421155 Jul 13, 2019 (153)
110 ILLUMINA ss3744421156 Jul 13, 2019 (153)
111 ILLUMINA ss3744910848 Jul 13, 2019 (153)
112 EVA ss3753179920 Jul 13, 2019 (153)
113 PAGE_CC ss3771835072 Jul 13, 2019 (153)
114 ILLUMINA ss3772409488 Jul 13, 2019 (153)
115 PACBIO ss3787868875 Jul 13, 2019 (153)
116 PACBIO ss3792877733 Jul 13, 2019 (153)
117 PACBIO ss3797762327 Jul 13, 2019 (153)
118 KHV_HUMAN_GENOMES ss3818496230 Jul 13, 2019 (153)
119 EVA ss3834273849 Apr 27, 2020 (154)
120 EVA ss3840735795 Apr 27, 2020 (154)
121 EVA ss3846224932 Apr 27, 2020 (154)
122 HGDP ss3847526359 Apr 27, 2020 (154)
123 SGDP_PRJ ss3883074458 Apr 27, 2020 (154)
124 KRGDB ss3932259286 Apr 27, 2020 (154)
125 KOGIC ss3976288923 Apr 27, 2020 (154)
126 1000Genomes NC_000015.9 - 61994134 Oct 12, 2018 (152)
127 The Avon Longitudinal Study of Parents and Children NC_000015.9 - 61994134 Oct 12, 2018 (152)
128 Genetic variation in the Estonian population NC_000015.9 - 61994134 Oct 12, 2018 (152)
129 The Danish reference pan genome NC_000015.9 - 61994134 Apr 27, 2020 (154)
130 gnomAD - Genomes NC_000015.9 - 61994134 Jul 13, 2019 (153)
131 Genome of the Netherlands Release 5 NC_000015.9 - 61994134 Apr 27, 2020 (154)
132 HGDP-CEPH-db Supplement 1 NC_000015.8 - 59781426 Apr 27, 2020 (154)
133 HapMap NC_000015.10 - 61701935 Apr 27, 2020 (154)
134 KOREAN population from KRGDB NC_000015.9 - 61994134 Apr 27, 2020 (154)
135 Korean Genome Project NC_000015.10 - 61701935 Apr 27, 2020 (154)
136 Northern Sweden NC_000015.9 - 61994134 Jul 13, 2019 (153)
137 The PAGE Study NC_000015.10 - 61701935 Jul 13, 2019 (153)
138 Qatari NC_000015.9 - 61994134 Apr 27, 2020 (154)
139 SGDP_PRJ NC_000015.9 - 61994134 Apr 27, 2020 (154)
140 Siberian NC_000015.9 - 61994134 Apr 27, 2020 (154)
141 TopMed NC_000015.10 - 61701935 Oct 12, 2018 (152)
142 UK 10K study - Twins NC_000015.9 - 61994134 Oct 12, 2018 (152)
143 A Vietnamese Genetic Variation Database NC_000015.9 - 61994134 Jul 13, 2019 (153)
144 dbGaP Population Frequency Project NC_000015.10 - 61701935 Apr 27, 2020 (154)
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)
rs57062719 May 23, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
204251, ss84827229, ss90183034, ss108879053, ss114284275, ss118256259, ss168163921, ss169693806, ss171216647, ss200935640, ss207209511, ss255043545, ss282286589, ss286967485, ss291735851, ss480562555, ss825464692, ss1695885015, ss1713495993, ss3639058159, ss3639534428, ss3643073971, ss3847526359 NC_000015.8:59781425:G:A NC_000015.10:61701934:G:A (self)
66848811, 37114382, 26288194, 3888637, 182400720, 16570148, 39436680, 14274328, 17312828, 35091438, 9336455, 37114382, 8257978, ss226932591, ss236806897, ss243189113, ss480576946, ss481396415, ss485076865, ss537088444, ss564526497, ss660257447, ss778495485, ss782984720, ss783945662, ss832241372, ss832900393, ss833951537, ss991863599, ss1080186503, ss1353766503, ss1427649981, ss1577661747, ss1633160246, ss1676154279, ss1752166759, ss1808238455, ss1935270898, ss1946395755, ss1959618480, ss1968127408, ss2028415348, ss2095059515, ss2156820101, ss2371834099, ss2628703241, ss2633239664, ss2701294350, ss2710818441, ss2935758526, ss3013403497, ss3021640129, ss3351150478, ss3625674876, ss3627378938, ss3631231758, ss3633100140, ss3633804843, ss3634610324, ss3635493695, ss3636300394, ss3637244982, ss3638090055, ss3640317645, ss3644648856, ss3652041259, ss3680549946, ss3740989463, ss3744132234, ss3744421155, ss3744421156, ss3744910848, ss3753179920, ss3772409488, ss3787868875, ss3792877733, ss3797762327, ss3834273849, ss3840735795, ss3883074458, ss3932259286 NC_000015.9:61994133:G:A NC_000015.10:61701934:G:A (self)
1279472, 32666924, 1056541, 131096549, 563405406, ss2207408648, ss3028032244, ss3229603873, ss3650371450, ss3698039558, ss3725506115, ss3771835072, ss3818496230, ss3846224932, ss3976288923 NC_000015.10:61701934:G:A NC_000015.10:61701934:G:A (self)
ss21246596 NT_010194.16:32784690:G:A NC_000015.10:61701934:G:A (self)
ss3381940, ss23812432, ss43770986, ss65996768, ss66743331, ss67252902, ss67650838, ss69178862, ss70731246, ss71300757, ss75727268, ss79134174, ss84047092, ss96764673, ss106435113, ss122030245, ss136384573, ss136881876, ss153910805, ss156632797, ss159388636, ss160545537, ss171248276, ss173334539 NT_010194.17:32784690:G:A NC_000015.10:61701934:G:A (self)
Help

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

6 citations for rs2414739
PMID Title Author Year Journal
26678010 Association of four new candidate genetic variants with Parkinson's disease in a Han Chinese population. Wang L et al. 2016 American journal of medical genetics. Part B, Neuropsychiatric genetics
26804608 Association of GCH1 and MIR4697, but not SIPA1L2 and VPS13C polymorphisms, with Parkinson's disease in Taiwan. Chen CM et al. 2016 Neurobiology of aging
27653855 SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case-control study. Safaralizadeh T et al. 2016 Journal of the neurological sciences
28380328 Polymorphism in MIR4697 but not VPS13C, GCH1, or SIPA1L2 is associated with risk of Parkinson's disease in a Han Chinese population. Yang X et al. 2017 Neuroscience letters
28927418 A systematic review and integrative approach to decode the common molecular link between levodopa response and Parkinson's disease. Guin D et al. 2017 BMC medical genomics
29622492 Association analyses of variants of SIPA1L2, MIR4697, GCH1, VPS13C, and DDRGK1 with Parkinson's disease in East Asians. Zou M et al. 2018 Neurobiology of aging
Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post557+f76c771