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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.

rs10492931

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:5187295 (GRCh38.p14) 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
A=0.466293 (123423/264690, TOPMED)
A=0.431033 (89604/207882, ALFA)
A=0.465955 (65203/139934, GnomAD) (+ 19 more)
A=0.40197 (11359/28258, 14KJPN)
A=0.40358 (6764/16760, 8.3KJPN)
A=0.4524 (2897/6404, 1000G_30x)
A=0.4531 (2269/5008, 1000G)
A=0.4112 (1842/4480, Estonian)
A=0.4255 (1640/3854, ALSPAC)
A=0.4223 (1566/3708, TWINSUK)
A=0.3836 (1124/2930, KOREAN)
A=0.4506 (939/2084, HGDP_Stanford)
A=0.4780 (805/1684, HapMap)
A=0.387 (386/998, GoNL)
A=0.393 (246/626, Chileans)
A=0.417 (250/600, NorthernSweden)
G=0.347 (129/372, SGDP_PRJ)
A=0.472 (102/216, Qatari)
G=0.491 (105/214, Vietnamese)
A=0.42 (17/40, GENOME_DK)
G=0.33 (10/30, Siberian)
G=0.38 (6/16, Ancient Sardinia)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
Publications
0 citations
Genomic View
See rs on genome

ALFA Allele Frequency
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: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 207882 G=0.568967 A=0.431033
European Sub 176904 G=0.570999 A=0.429001
African Sub 7770 G=0.4387 A=0.5613
African Others Sub 276 G=0.402 A=0.598
African American Sub 7494 G=0.4401 A=0.5599
Asian Sub 750 G=0.592 A=0.408
East Asian Sub 572 G=0.607 A=0.393
Other Asian Sub 178 G=0.545 A=0.455
Latin American 1 Sub 990 G=0.524 A=0.476
Latin American 2 Sub 9056 G=0.6144 A=0.3856
South Asian Sub 5052 G=0.6265 A=0.3735
Other Sub 7360 G=0.5659 A=0.4341


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
TopMed Global Study-wide 264690 G=0.533707 A=0.466293
Allele Frequency Aggregator Total Global 207882 G=0.568967 A=0.431033
Allele Frequency Aggregator European Sub 176904 G=0.570999 A=0.429001
Allele Frequency Aggregator Latin American 2 Sub 9056 G=0.6144 A=0.3856
Allele Frequency Aggregator African Sub 7770 G=0.4387 A=0.5613
Allele Frequency Aggregator Other Sub 7360 G=0.5659 A=0.4341
Allele Frequency Aggregator South Asian Sub 5052 G=0.6265 A=0.3735
Allele Frequency Aggregator Latin American 1 Sub 990 G=0.524 A=0.476
Allele Frequency Aggregator Asian Sub 750 G=0.592 A=0.408
gnomAD - Genomes Global Study-wide 139934 G=0.534045 A=0.465955
gnomAD - Genomes European Sub 75820 G=0.58132 A=0.41868
gnomAD - Genomes African Sub 41908 G=0.43906 A=0.56094
gnomAD - Genomes American Sub 13614 G=0.56868 A=0.43132
gnomAD - Genomes Ashkenazi Jewish Sub 3320 G=0.4708 A=0.5292
gnomAD - Genomes East Asian Sub 3122 G=0.5942 A=0.4058
gnomAD - Genomes Other Sub 2150 G=0.5093 A=0.4907
14KJPN JAPANESE Study-wide 28258 G=0.59803 A=0.40197
8.3KJPN JAPANESE Study-wide 16760 G=0.59642 A=0.40358
1000Genomes_30x Global Study-wide 6404 G=0.5476 A=0.4524
1000Genomes_30x African Sub 1786 G=0.4082 A=0.5918
1000Genomes_30x Europe Sub 1266 G=0.5585 A=0.4415
1000Genomes_30x South Asian Sub 1202 G=0.6040 A=0.3960
1000Genomes_30x East Asian Sub 1170 G=0.6308 A=0.3692
1000Genomes_30x American Sub 980 G=0.619 A=0.381
1000Genomes Global Study-wide 5008 G=0.5469 A=0.4531
1000Genomes African Sub 1322 G=0.3941 A=0.6059
1000Genomes East Asian Sub 1008 G=0.6359 A=0.3641
1000Genomes Europe Sub 1006 G=0.5497 A=0.4503
1000Genomes South Asian Sub 978 G=0.610 A=0.390
1000Genomes American Sub 694 G=0.615 A=0.385
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.5888 A=0.4112
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.5745 A=0.4255
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.5777 A=0.4223
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.6164 A=0.3836
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.5494 A=0.4506
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.640 A=0.360
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.587 A=0.413
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.469 A=0.531
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.541 A=0.459
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.421 A=0.579
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.560 A=0.440
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.57 A=0.43
HapMap Global Study-wide 1684 G=0.5220 A=0.4780
HapMap American Sub 756 G=0.593 A=0.407
HapMap African Sub 674 G=0.402 A=0.598
HapMap Asian Sub 254 G=0.630 A=0.370
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.613 A=0.387
Chileans Chilean Study-wide 626 G=0.607 A=0.393
Northern Sweden ACPOP Study-wide 600 G=0.583 A=0.417
SGDP_PRJ Global Study-wide 372 G=0.347 A=0.653
Qatari Global Study-wide 216 G=0.528 A=0.472
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.491 A=0.509
The Danish reference pan genome Danish Study-wide 40 G=0.57 A=0.42
Siberian Global Study-wide 30 G=0.33 A=0.67
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 16 G=0.38 A=0.62
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.p14 chr 1 NC_000001.11:g.5187295G>A
GRCh37.p13 chr 1 NC_000001.10:g.5247355G>A
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
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.p14 chr 1 NC_000001.11:g.5187295= NC_000001.11:g.5187295G>A
GRCh37.p13 chr 1 NC_000001.10:g.5247355= NC_000001.10:g.5247355G>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#.

119 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 PERLEGEN ss14881703 Dec 05, 2003 (119)
2 SSAHASNP ss20593128 Apr 05, 2004 (121)
3 PERLEGEN ss24238581 Sep 20, 2004 (123)
4 AFFY ss65919770 Dec 02, 2006 (127)
5 ILLUMINA ss66549306 Dec 02, 2006 (127)
6 ILLUMINA ss66887570 Dec 02, 2006 (127)
7 ILLUMINA ss66987242 Dec 02, 2006 (127)
8 PERLEGEN ss68757279 May 18, 2007 (127)
9 ILLUMINA ss70369095 May 18, 2007 (127)
10 ILLUMINA ss70483421 May 23, 2008 (130)
11 ILLUMINA ss71007395 May 18, 2007 (127)
12 ILLUMINA ss75612906 Dec 07, 2007 (129)
13 AFFY ss76473098 Dec 07, 2007 (129)
14 KRIBB_YJKIM ss84951982 Dec 14, 2007 (130)
15 HUMANGENOME_JCVI ss99182665 Feb 04, 2009 (130)
16 BGI ss102715968 Dec 01, 2009 (131)
17 1000GENOMES ss107959941 Jan 22, 2009 (130)
18 1000GENOMES ss109988520 Jan 24, 2009 (130)
19 ILLUMINA-UK ss118464199 Feb 14, 2009 (130)
20 ILLUMINA ss121325487 Dec 01, 2009 (131)
21 ENSEMBL ss143421456 Dec 01, 2009 (131)
22 ILLUMINA ss152749984 Dec 01, 2009 (131)
23 GMI ss154577300 Dec 01, 2009 (131)
24 ILLUMINA ss159128319 Dec 01, 2009 (131)
25 ILLUMINA ss159900985 Dec 01, 2009 (131)
26 COMPLETE_GENOMICS ss163019009 Jul 04, 2010 (132)
27 COMPLETE_GENOMICS ss166033778 Jul 04, 2010 (132)
28 ILLUMINA ss169441650 Jul 04, 2010 (132)
29 ILLUMINA ss170190441 Jul 04, 2010 (132)
30 BUSHMAN ss197946929 Jul 04, 2010 (132)
31 1000GENOMES ss218211150 Jul 14, 2010 (132)
32 1000GENOMES ss230410217 Jul 14, 2010 (132)
33 1000GENOMES ss238128238 Jul 15, 2010 (132)
34 GMI ss275697023 May 04, 2012 (137)
35 GMI ss283993875 Apr 25, 2013 (138)
36 ILLUMINA ss479288167 May 04, 2012 (137)
37 ILLUMINA ss479291207 May 04, 2012 (137)
38 ILLUMINA ss479669919 Sep 08, 2015 (146)
39 ILLUMINA ss484444562 May 04, 2012 (137)
40 ILLUMINA ss536612682 Sep 08, 2015 (146)
41 TISHKOFF ss553746241 Apr 25, 2013 (138)
42 SSMP ss647545886 Apr 25, 2013 (138)
43 ILLUMINA ss778733623 Sep 08, 2015 (146)
44 ILLUMINA ss782668788 Sep 08, 2015 (146)
45 ILLUMINA ss783637533 Sep 08, 2015 (146)
46 ILLUMINA ss825338706 Apr 01, 2015 (144)
47 ILLUMINA ss831919423 Sep 08, 2015 (146)
48 ILLUMINA ss832641012 Jul 12, 2019 (153)
49 ILLUMINA ss834193139 Sep 08, 2015 (146)
50 EVA-GONL ss974809740 Aug 21, 2014 (142)
51 JMKIDD_LAB ss1067637554 Aug 21, 2014 (142)
52 1000GENOMES ss1289499036 Aug 21, 2014 (142)
53 DDI ss1425698167 Apr 01, 2015 (144)
54 EVA_GENOME_DK ss1573865887 Apr 01, 2015 (144)
55 EVA_DECODE ss1584168447 Apr 01, 2015 (144)
56 EVA_UK10K_ALSPAC ss1599453377 Apr 01, 2015 (144)
57 EVA_UK10K_TWINSUK ss1642447410 Apr 01, 2015 (144)
58 EVA_SVP ss1712307970 Apr 01, 2015 (144)
59 ILLUMINA ss1751923688 Sep 08, 2015 (146)
60 HAMMER_LAB ss1793812009 Sep 08, 2015 (146)
61 WEILL_CORNELL_DGM ss1918006118 Feb 12, 2016 (147)
62 GENOMED ss1966674994 Jul 19, 2016 (147)
63 JJLAB ss2019519532 Sep 14, 2016 (149)
64 USC_VALOUEV ss2147510916 Dec 20, 2016 (150)
65 HUMAN_LONGEVITY ss2159669804 Dec 20, 2016 (150)
66 ILLUMINA ss2632470833 Nov 08, 2017 (151)
67 ILLUMINA ss2634995623 Nov 08, 2017 (151)
68 GRF ss2697405774 Nov 08, 2017 (151)
69 GNOMAD ss2751097451 Nov 08, 2017 (151)
70 SWEGEN ss2986220994 Nov 08, 2017 (151)
71 BIOINF_KMB_FNS_UNIBA ss3023524041 Nov 08, 2017 (151)
72 CSHL ss3343296069 Nov 08, 2017 (151)
73 ILLUMINA ss3626015132 Oct 11, 2018 (152)
74 ILLUMINA ss3630509978 Oct 11, 2018 (152)
75 ILLUMINA ss3632879157 Oct 11, 2018 (152)
76 ILLUMINA ss3633572834 Oct 11, 2018 (152)
77 ILLUMINA ss3634304204 Oct 11, 2018 (152)
78 ILLUMINA ss3635266993 Oct 11, 2018 (152)
79 ILLUMINA ss3635980583 Oct 11, 2018 (152)
80 ILLUMINA ss3637017353 Oct 11, 2018 (152)
81 ILLUMINA ss3637734529 Oct 11, 2018 (152)
82 ILLUMINA ss3638888740 Oct 11, 2018 (152)
83 ILLUMINA ss3639441138 Oct 11, 2018 (152)
84 ILLUMINA ss3640011569 Oct 11, 2018 (152)
85 ILLUMINA ss3642748660 Oct 11, 2018 (152)
86 URBANLAB ss3646590096 Oct 11, 2018 (152)
87 EGCUT_WGS ss3654322403 Jul 12, 2019 (153)
88 EVA_DECODE ss3686071665 Jul 12, 2019 (153)
89 ACPOP ss3726751595 Jul 12, 2019 (153)
90 ILLUMINA ss3744605191 Jul 12, 2019 (153)
91 EVA ss3745772065 Jul 12, 2019 (153)
92 ILLUMINA ss3772106845 Jul 12, 2019 (153)
93 PACBIO ss3783312547 Jul 12, 2019 (153)
94 PACBIO ss3788989204 Jul 12, 2019 (153)
95 PACBIO ss3793861852 Jul 12, 2019 (153)
96 KHV_HUMAN_GENOMES ss3798793019 Jul 12, 2019 (153)
97 EVA ss3826001204 Apr 25, 2020 (154)
98 EVA ss3836387884 Apr 25, 2020 (154)
99 EVA ss3841792093 Apr 25, 2020 (154)
100 HGDP ss3847323109 Apr 25, 2020 (154)
101 SGDP_PRJ ss3848096618 Apr 25, 2020 (154)
102 KRGDB ss3892959926 Apr 25, 2020 (154)
103 EVA ss3984775963 Apr 25, 2021 (155)
104 EVA ss4016890876 Apr 25, 2021 (155)
105 TOPMED ss4437679208 Apr 25, 2021 (155)
106 TOMMO_GENOMICS ss5142254601 Apr 25, 2021 (155)
107 1000G_HIGH_COVERAGE ss5241009705 Oct 12, 2022 (156)
108 EVA ss5314589241 Oct 12, 2022 (156)
109 EVA ss5316450154 Oct 12, 2022 (156)
110 HUGCELL_USP ss5442230792 Oct 12, 2022 (156)
111 1000G_HIGH_COVERAGE ss5512694307 Oct 12, 2022 (156)
112 SANFORD_IMAGENETICS ss5624833181 Oct 12, 2022 (156)
113 TOMMO_GENOMICS ss5666484477 Oct 12, 2022 (156)
114 EVA ss5799473657 Oct 12, 2022 (156)
115 YY_MCH ss5800283366 Oct 12, 2022 (156)
116 EVA ss5831477391 Oct 12, 2022 (156)
117 EVA ss5848765510 Oct 12, 2022 (156)
118 EVA ss5906858674 Oct 12, 2022 (156)
119 EVA ss5936659203 Oct 12, 2022 (156)
120 1000Genomes NC_000001.10 - 5247355 Oct 11, 2018 (152)
121 1000Genomes_30x NC_000001.11 - 5187295 Oct 12, 2022 (156)
122 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 5247355 Oct 11, 2018 (152)
123 Chileans NC_000001.10 - 5247355 Apr 25, 2020 (154)
124 Genetic variation in the Estonian population NC_000001.10 - 5247355 Oct 11, 2018 (152)
125 The Danish reference pan genome NC_000001.10 - 5247355 Apr 25, 2020 (154)
126 gnomAD - Genomes NC_000001.11 - 5187295 Apr 25, 2021 (155)
127 Genome of the Netherlands Release 5 NC_000001.10 - 5247355 Apr 25, 2020 (154)
128 HGDP-CEPH-db Supplement 1 NC_000001.9 - 5147215 Apr 25, 2020 (154)
129 HapMap NC_000001.11 - 5187295 Apr 25, 2020 (154)
130 KOREAN population from KRGDB NC_000001.10 - 5247355 Apr 25, 2020 (154)
131 Northern Sweden NC_000001.10 - 5247355 Jul 12, 2019 (153)
132 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 5247355 Apr 25, 2021 (155)
133 Qatari NC_000001.10 - 5247355 Apr 25, 2020 (154)
134 SGDP_PRJ NC_000001.10 - 5247355 Apr 25, 2020 (154)
135 Siberian NC_000001.10 - 5247355 Apr 25, 2020 (154)
136 8.3KJPN NC_000001.10 - 5247355 Apr 25, 2021 (155)
137 14KJPN NC_000001.11 - 5187295 Oct 12, 2022 (156)
138 TopMed NC_000001.11 - 5187295 Apr 25, 2021 (155)
139 UK 10K study - Twins NC_000001.10 - 5247355 Oct 11, 2018 (152)
140 A Vietnamese Genetic Variation Database NC_000001.10 - 5247355 Jul 12, 2019 (153)
141 ALFA NC_000001.11 - 5187295 Apr 25, 2021 (155)
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)
rs17375400 Oct 07, 2004 (123)
rs57515725 May 23, 2008 (130)
rs386513627 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss3638888740, ss3639441138 NC_000001.8:5157727:G:A NC_000001.11:5187294:G:A (self)
1001, ss107959941, ss109988520, ss118464199, ss163019009, ss166033778, ss197946929, ss275697023, ss283993875, ss479288167, ss825338706, ss1584168447, ss1712307970, ss2634995623, ss3642748660, ss3847323109 NC_000001.9:5147214:G:A NC_000001.11:5187294:G:A (self)
168546, 81807, 717, 60651, 1373121, 36059, 137320, 36460, 1890, 48048, 113598, 27270, 223908, 81807, 18326, ss218211150, ss230410217, ss238128238, ss479291207, ss479669919, ss484444562, ss536612682, ss553746241, ss647545886, ss778733623, ss782668788, ss783637533, ss831919423, ss832641012, ss834193139, ss974809740, ss1067637554, ss1289499036, ss1425698167, ss1573865887, ss1599453377, ss1642447410, ss1751923688, ss1793812009, ss1918006118, ss1966674994, ss2019519532, ss2147510916, ss2632470833, ss2697405774, ss2751097451, ss2986220994, ss3343296069, ss3626015132, ss3630509978, ss3632879157, ss3633572834, ss3634304204, ss3635266993, ss3635980583, ss3637017353, ss3637734529, ss3640011569, ss3654322403, ss3726751595, ss3744605191, ss3745772065, ss3772106845, ss3783312547, ss3788989204, ss3793861852, ss3826001204, ss3836387884, ss3848096618, ss3892959926, ss3984775963, ss4016890876, ss5142254601, ss5314589241, ss5316450154, ss5624833181, ss5799473657, ss5831477391, ss5936659203 NC_000001.10:5247354:G:A NC_000001.11:5187294:G:A (self)
220242, 1177663, 5772, 321581, 1285543, 12616207581, ss2159669804, ss3023524041, ss3646590096, ss3686071665, ss3798793019, ss3841792093, ss4437679208, ss5241009705, ss5442230792, ss5512694307, ss5666484477, ss5800283366, ss5848765510, ss5906858674 NC_000001.11:5187294:G:A NC_000001.11:5187294:G:A (self)
ss20593128 NT_004547.16:1250987:G:A NC_000001.11:5187294:G:A (self)
ss14881703, ss24238581, ss65919770, ss66549306, ss66887570, ss66987242, ss68757279, ss70369095, ss70483421, ss71007395, ss75612906, ss76473098, ss84951982, ss99182665, ss102715968, ss121325487, ss143421456, ss152749984, ss154577300, ss159128319, ss159900985, ss169441650, ss170190441 NT_021937.19:1252086:G:A NC_000001.11:5187294: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.

No publications for rs10492931

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.post761+d5e8e07