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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.

rs1000989

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr13:110174956 (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
T>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.336662 (89111/264690, TOPMED)
C=0.338835 (47447/140030, GnomAD)
C=0.35822 (26887/75058, ALFA) (+ 20 more)
C=0.24485 (6919/28258, 14KJPN)
C=0.24505 (4107/16760, 8.3KJPN)
C=0.3154 (2020/6404, 1000G_30x)
C=0.3173 (1589/5008, 1000G)
C=0.3835 (1718/4480, Estonian)
C=0.3736 (1440/3854, ALSPAC)
C=0.3714 (1377/3708, TWINSUK)
C=0.2447 (717/2930, KOREAN)
C=0.3364 (701/2084, HGDP_Stanford)
C=0.2391 (438/1832, Korea1K)
C=0.2956 (522/1766, HapMap)
C=0.363 (362/998, GoNL)
C=0.305 (191/626, Chileans)
C=0.408 (245/600, NorthernSweden)
T=0.370 (123/332, SGDP_PRJ)
C=0.236 (51/216, Qatari)
C=0.403 (87/216, Vietnamese)
C=0.27 (26/96, Ancient Sardinia)
C=0.30 (12/40, GENOME_DK)
T=0.32 (7/22, Siberian)
Clinical Significance
Reported in ClinVar
Gene : Consequence
COL4A1 : Intron Variant
Publications
1 citation
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 75058 T=0.64178 C=0.35822
European Sub 58758 T=0.63428 C=0.36572
African Sub 5200 T=0.7240 C=0.2760
African Others Sub 182 T=0.742 C=0.258
African American Sub 5018 T=0.7234 C=0.2766
Asian Sub 238 T=0.664 C=0.336
East Asian Sub 164 T=0.665 C=0.335
Other Asian Sub 74 T=0.66 C=0.34
Latin American 1 Sub 396 T=0.689 C=0.311
Latin American 2 Sub 3382 T=0.6067 C=0.3933
South Asian Sub 4968 T=0.6608 C=0.3392
Other Sub 2116 T=0.6479 C=0.3521


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 T=0.663338 C=0.336662
gnomAD - Genomes Global Study-wide 140030 T=0.661165 C=0.338835
gnomAD - Genomes European Sub 75836 T=0.63080 C=0.36920
gnomAD - Genomes African Sub 41962 T=0.72206 C=0.27794
gnomAD - Genomes American Sub 13644 T=0.63838 C=0.36162
gnomAD - Genomes Ashkenazi Jewish Sub 3320 T=0.6551 C=0.3449
gnomAD - Genomes East Asian Sub 3118 T=0.6908 C=0.3092
gnomAD - Genomes Other Sub 2150 T=0.6549 C=0.3451
Allele Frequency Aggregator Total Global 75058 T=0.64178 C=0.35822
Allele Frequency Aggregator European Sub 58758 T=0.63428 C=0.36572
Allele Frequency Aggregator African Sub 5200 T=0.7240 C=0.2760
Allele Frequency Aggregator South Asian Sub 4968 T=0.6608 C=0.3392
Allele Frequency Aggregator Latin American 2 Sub 3382 T=0.6067 C=0.3933
Allele Frequency Aggregator Other Sub 2116 T=0.6479 C=0.3521
Allele Frequency Aggregator Latin American 1 Sub 396 T=0.689 C=0.311
Allele Frequency Aggregator Asian Sub 238 T=0.664 C=0.336
14KJPN JAPANESE Study-wide 28258 T=0.75515 C=0.24485
8.3KJPN JAPANESE Study-wide 16760 T=0.75495 C=0.24505
1000Genomes_30x Global Study-wide 6404 T=0.6846 C=0.3154
1000Genomes_30x African Sub 1786 T=0.7374 C=0.2626
1000Genomes_30x Europe Sub 1266 T=0.6453 C=0.3547
1000Genomes_30x South Asian Sub 1202 T=0.6290 C=0.3710
1000Genomes_30x East Asian Sub 1170 T=0.7282 C=0.2718
1000Genomes_30x American Sub 980 T=0.655 C=0.345
1000Genomes Global Study-wide 5008 T=0.6827 C=0.3173
1000Genomes African Sub 1322 T=0.7474 C=0.2526
1000Genomes East Asian Sub 1008 T=0.7222 C=0.2778
1000Genomes Europe Sub 1006 T=0.6332 C=0.3668
1000Genomes South Asian Sub 978 T=0.630 C=0.370
1000Genomes American Sub 694 T=0.648 C=0.352
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.6165 C=0.3835
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.6264 C=0.3736
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.6286 C=0.3714
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.7553 C=0.2447
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 T=0.6636 C=0.3364
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 T=0.721 C=0.279
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 T=0.681 C=0.319
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 T=0.680 C=0.320
HGDP-CEPH-db Supplement 1 Europe Sub 320 T=0.650 C=0.350
HGDP-CEPH-db Supplement 1 Africa Sub 242 T=0.707 C=0.293
HGDP-CEPH-db Supplement 1 America Sub 216 T=0.537 C=0.463
HGDP-CEPH-db Supplement 1 Oceania Sub 72 T=0.40 C=0.60
Korean Genome Project KOREAN Study-wide 1832 T=0.7609 C=0.2391
HapMap Global Study-wide 1766 T=0.7044 C=0.2956
HapMap American Sub 768 T=0.643 C=0.357
HapMap African Sub 568 T=0.783 C=0.217
HapMap Asian Sub 254 T=0.768 C=0.232
HapMap Europe Sub 176 T=0.625 C=0.375
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.637 C=0.363
Chileans Chilean Study-wide 626 T=0.695 C=0.305
Northern Sweden ACPOP Study-wide 600 T=0.592 C=0.408
SGDP_PRJ Global Study-wide 332 T=0.370 C=0.630
Qatari Global Study-wide 216 T=0.764 C=0.236
A Vietnamese Genetic Variation Database Global Study-wide 216 T=0.597 C=0.403
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 96 T=0.73 C=0.27
The Danish reference pan genome Danish Study-wide 40 T=0.70 C=0.30
Siberian Global Study-wide 22 T=0.32 C=0.68
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 13 NC_000013.11:g.110174956T>C
GRCh37.p13 chr 13 NC_000013.10:g.110827303T>C
COL4A1 RefSeqGene (LRG_1116) NG_011544.2:g.137194A>G
Gene: COL4A1, collagen type IV alpha 1 chain (minus strand)
Molecule type Change Amino acid[Codon] SO Term
COL4A1 transcript variant 1 NM_001845.6:c.3199-207A>G N/A Intron Variant
COL4A1 transcript variant 2 NM_001303110.2:c. N/A Genic Downstream 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.

Allele: C (allele ID: 1259380 )
ClinVar Accession Disease Names Clinical Significance
RCV001684626.1 not provided Benign
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 T= C
GRCh38.p14 chr 13 NC_000013.11:g.110174956= NC_000013.11:g.110174956T>C
GRCh37.p13 chr 13 NC_000013.10:g.110827303= NC_000013.10:g.110827303T>C
COL4A1 RefSeqGene (LRG_1116) NG_011544.2:g.137194= NG_011544.2:g.137194A>G
COL4A1 transcript NM_001845.4:c.3199-207= NM_001845.4:c.3199-207A>G
COL4A1 transcript variant 1 NM_001845.6:c.3199-207= NM_001845.6:c.3199-207A>G
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#.

100 SubSNP, 23 Frequency, 1 ClinVar submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss1461108 Oct 05, 2000 (86)
2 SC_SNP ss13190378 Dec 05, 2003 (119)
3 CSHL-HAPMAP ss16622410 Feb 27, 2004 (120)
4 ABI ss43467167 Mar 13, 2006 (126)
5 ILLUMINA ss65714009 Oct 16, 2006 (127)
6 ILLUMINA ss66761734 Dec 02, 2006 (127)
7 ILLUMINA ss66864206 Dec 02, 2006 (127)
8 ILLUMINA ss66933590 Dec 02, 2006 (127)
9 ILLUMINA ss70356102 May 18, 2007 (127)
10 ILLUMINA ss70459568 May 23, 2008 (130)
11 ILLUMINA ss70980152 May 18, 2007 (127)
12 ILLUMINA ss75726932 Dec 06, 2007 (129)
13 AFFY ss76766213 Dec 08, 2007 (130)
14 HGSV ss77347897 Dec 06, 2007 (129)
15 HGSV ss82973579 Dec 14, 2007 (130)
16 KRIBB_YJKIM ss83650732 Dec 14, 2007 (130)
17 BGI ss103162736 Dec 01, 2009 (131)
18 1000GENOMES ss108115615 Jan 22, 2009 (130)
19 1000GENOMES ss115314961 Jan 25, 2009 (130)
20 ILLUMINA ss121252522 Dec 01, 2009 (131)
21 ILLUMINA ss152540573 Dec 01, 2009 (131)
22 ILLUMINA ss159103424 Dec 01, 2009 (131)
23 ENSEMBL ss161573486 Dec 01, 2009 (131)
24 COMPLETE_GENOMICS ss168686428 Jul 04, 2010 (132)
25 ILLUMINA ss169209325 Jul 04, 2010 (132)
26 ILLUMINA ss169501964 Jul 04, 2010 (132)
27 COMPLETE_GENOMICS ss170796774 Jul 04, 2010 (132)
28 COMPLETE_GENOMICS ss171746198 Jul 04, 2010 (132)
29 BUSHMAN ss199726407 Jul 04, 2010 (132)
30 1000GENOMES ss226423535 Jul 14, 2010 (132)
31 1000GENOMES ss236433914 Jul 15, 2010 (132)
32 1000GENOMES ss242889828 Jul 15, 2010 (132)
33 ILLUMINA ss244267469 Jul 04, 2010 (132)
34 BL ss255321928 May 09, 2011 (134)
35 GMI ss281888255 May 04, 2012 (137)
36 GMI ss286789587 Apr 25, 2013 (138)
37 PJP ss291537492 May 09, 2011 (134)
38 ILLUMINA ss410884236 Sep 17, 2011 (135)
39 ILLUMINA ss536564992 Sep 08, 2015 (146)
40 TISHKOFF ss563926561 Apr 25, 2013 (138)
41 SSMP ss659574382 Apr 25, 2013 (138)
42 ILLUMINA ss825325833 Apr 01, 2015 (144)
43 ILLUMINA ss832616220 Aug 21, 2014 (142)
44 ILLUMINA ss833206909 Aug 21, 2014 (142)
45 EVA-GONL ss990856549 Aug 21, 2014 (142)
46 JMKIDD_LAB ss1079441792 Aug 21, 2014 (142)
47 1000GENOMES ss1349919062 Aug 21, 2014 (142)
48 DDI ss1427330255 Apr 01, 2015 (144)
49 EVA_GENOME_DK ss1577076144 Apr 01, 2015 (144)
50 EVA_UK10K_ALSPAC ss1631181133 Apr 01, 2015 (144)
51 EVA_UK10K_TWINSUK ss1674175166 Apr 01, 2015 (144)
52 EVA_SVP ss1713424509 Apr 01, 2015 (144)
53 HAMMER_LAB ss1807798826 Sep 08, 2015 (146)
54 WEILL_CORNELL_DGM ss1934218973 Feb 12, 2016 (147)
55 GENOMED ss1967897850 Jul 19, 2016 (147)
56 JJLAB ss2027885553 Sep 14, 2016 (149)
57 USC_VALOUEV ss2156252821 Dec 20, 2016 (150)
58 HUMAN_LONGEVITY ss2199826004 Dec 20, 2016 (150)
59 SYSTEMSBIOZJU ss2628431270 Nov 08, 2017 (151)
60 ILLUMINA ss2635049205 Nov 08, 2017 (151)
61 GRF ss2700652235 Nov 08, 2017 (151)
62 GNOMAD ss2924481801 Nov 08, 2017 (151)
63 SWEGEN ss3011718924 Nov 08, 2017 (151)
64 BIOINF_KMB_FNS_UNIBA ss3027765795 Nov 08, 2017 (151)
65 CSHL ss3350666470 Nov 08, 2017 (151)
66 ILLUMINA ss3627157471 Oct 12, 2018 (152)
67 ILLUMINA ss3638034788 Oct 12, 2018 (152)
68 ILLUMINA ss3639031111 Oct 12, 2018 (152)
69 ILLUMINA ss3639519812 Oct 12, 2018 (152)
70 ILLUMINA ss3643022794 Oct 12, 2018 (152)
71 EGCUT_WGS ss3679011373 Jul 13, 2019 (153)
72 EVA_DECODE ss3696140489 Jul 13, 2019 (153)
73 ACPOP ss3740136404 Jul 13, 2019 (153)
74 EVA ss3751989768 Jul 13, 2019 (153)
75 PACBIO ss3787584382 Jul 13, 2019 (153)
76 PACBIO ss3792633851 Jul 13, 2019 (153)
77 PACBIO ss3797517818 Jul 13, 2019 (153)
78 KHV_HUMAN_GENOMES ss3817323455 Jul 13, 2019 (153)
79 EVA ss3833775502 Apr 27, 2020 (154)
80 HGDP ss3847494166 Apr 27, 2020 (154)
81 SGDP_PRJ ss3880877436 Apr 27, 2020 (154)
82 KRGDB ss3929810735 Apr 27, 2020 (154)
83 KOGIC ss3974365958 Apr 27, 2020 (154)
84 EVA ss3985664307 Apr 26, 2021 (155)
85 EVA ss4017655912 Apr 26, 2021 (155)
86 TOPMED ss4961503768 Apr 26, 2021 (155)
87 TOMMO_GENOMICS ss5211912915 Apr 26, 2021 (155)
88 1000G_HIGH_COVERAGE ss5295222834 Oct 16, 2022 (156)
89 EVA ss5413495110 Oct 16, 2022 (156)
90 HUGCELL_USP ss5489439219 Oct 16, 2022 (156)
91 EVA ss5511146512 Oct 16, 2022 (156)
92 1000G_HIGH_COVERAGE ss5595007378 Oct 16, 2022 (156)
93 SANFORD_IMAGENETICS ss5655641966 Oct 16, 2022 (156)
94 TOMMO_GENOMICS ss5764314153 Oct 16, 2022 (156)
95 YY_MCH ss5814491988 Oct 16, 2022 (156)
96 EVA ss5840069090 Oct 16, 2022 (156)
97 EVA ss5850918843 Oct 16, 2022 (156)
98 EVA ss5926814166 Oct 16, 2022 (156)
99 EVA ss5947091141 Oct 16, 2022 (156)
100 EVA ss5981282405 Oct 16, 2022 (156)
101 1000Genomes NC_000013.10 - 110827303 Oct 12, 2018 (152)
102 1000Genomes_30x NC_000013.11 - 110174956 Oct 16, 2022 (156)
103 The Avon Longitudinal Study of Parents and Children NC_000013.10 - 110827303 Oct 12, 2018 (152)
104 Chileans NC_000013.10 - 110827303 Apr 27, 2020 (154)
105 Genetic variation in the Estonian population NC_000013.10 - 110827303 Oct 12, 2018 (152)
106 The Danish reference pan genome NC_000013.10 - 110827303 Apr 27, 2020 (154)
107 gnomAD - Genomes NC_000013.11 - 110174956 Apr 26, 2021 (155)
108 Genome of the Netherlands Release 5 NC_000013.10 - 110827303 Apr 27, 2020 (154)
109 HGDP-CEPH-db Supplement 1 NC_000013.9 - 109625304 Apr 27, 2020 (154)
110 HapMap NC_000013.11 - 110174956 Apr 27, 2020 (154)
111 KOREAN population from KRGDB NC_000013.10 - 110827303 Apr 27, 2020 (154)
112 Korean Genome Project NC_000013.11 - 110174956 Apr 27, 2020 (154)
113 Northern Sweden NC_000013.10 - 110827303 Jul 13, 2019 (153)
114 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000013.10 - 110827303 Apr 26, 2021 (155)
115 Qatari NC_000013.10 - 110827303 Apr 27, 2020 (154)
116 SGDP_PRJ NC_000013.10 - 110827303 Apr 27, 2020 (154)
117 Siberian NC_000013.10 - 110827303 Apr 27, 2020 (154)
118 8.3KJPN NC_000013.10 - 110827303 Apr 26, 2021 (155)
119 14KJPN NC_000013.11 - 110174956 Oct 16, 2022 (156)
120 TopMed NC_000013.11 - 110174956 Apr 26, 2021 (155)
121 UK 10K study - Twins NC_000013.10 - 110827303 Oct 12, 2018 (152)
122 A Vietnamese Genetic Variation Database NC_000013.10 - 110827303 Jul 13, 2019 (153)
123 ALFA NC_000013.11 - 110174956 Apr 26, 2021 (155)
124 ClinVar RCV001684626.1 Oct 16, 2022 (156)
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)
rs56507229 May 23, 2008 (130)
rs56772210 May 23, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
172058, ss76766213, ss77347897, ss82973579, ss108115615, ss115314961, ss168686428, ss170796774, ss171746198, ss199726407, ss244267469, ss255321928, ss281888255, ss286789587, ss291537492, ss410884236, ss825325833, ss1713424509, ss2635049205, ss3639031111, ss3639519812, ss3643022794, ss3847494166 NC_000013.9:109625303:T:C NC_000013.11:110174955:T:C (self)
62858354, 34932903, 131557, 24749621, 3487570, 15597874, 36988129, 13421269, 890234, 16260903, 32894416, 8769175, 69882222, 34932903, 7768513, ss226423535, ss236433914, ss242889828, ss536564992, ss563926561, ss659574382, ss832616220, ss833206909, ss990856549, ss1079441792, ss1349919062, ss1427330255, ss1577076144, ss1631181133, ss1674175166, ss1807798826, ss1934218973, ss1967897850, ss2027885553, ss2156252821, ss2628431270, ss2700652235, ss2924481801, ss3011718924, ss3350666470, ss3627157471, ss3638034788, ss3679011373, ss3740136404, ss3751989768, ss3787584382, ss3792633851, ss3797517818, ss3833775502, ss3880877436, ss3929810735, ss3985664307, ss4017655912, ss5211912915, ss5413495110, ss5511146512, ss5655641966, ss5840069090, ss5947091141, ss5981282405 NC_000013.10:110827302:T:C NC_000013.11:110174955:T:C (self)
RCV001684626.1, 82533313, 443203256, 1091000, 30743959, 98151257, 177049426, 3170770502, ss2199826004, ss3027765795, ss3696140489, ss3817323455, ss3974365958, ss4961503768, ss5295222834, ss5489439219, ss5595007378, ss5764314153, ss5814491988, ss5850918843, ss5926814166 NC_000013.11:110174955:T:C NC_000013.11:110174955:T:C (self)
ss13190378 NT_009952.13:23916978:T:C NC_000013.11:110174955:T:C (self)
ss1461108, ss16622410, ss43467167, ss65714009, ss66761734, ss66864206, ss66933590, ss70356102, ss70459568, ss70980152, ss75726932, ss83650732, ss103162736, ss121252522, ss152540573, ss159103424, ss161573486, ss169209325, ss169501964 NT_009952.14:23916978:T:C NC_000013.11:110174955:T:C (self)
Help

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

1 citation for rs1000989
PMID Title Author Year Journal
26860460 Gene signatures of postoperative atrial fibrillation in atrial tissue after coronary artery bypass grafting surgery in patients receiving β-blockers. Kertai MD et al. 2016 Journal of molecular and cellular cardiology
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