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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs6721964

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr2:190713628 (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 / G>C
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.327889 (86789/264690, TOPMED)
G=0.338268 (82256/243168, ALFA)
G=0.319921 (44796/140022, GnomAD) (+ 18 more)
G=0.35053 (27587/78700, PAGE_STUDY)
G=0.43541 (12303/28256, 14KJPN)
G=0.43735 (7330/16760, 8.3KJPN)
G=0.4012 (2569/6404, 1000G_30x)
G=0.4034 (2020/5008, 1000G)
G=0.3779 (1693/4480, Estonian)
G=0.3326 (1282/3854, ALSPAC)
G=0.3220 (1194/3708, TWINSUK)
G=0.3802 (1114/2930, KOREAN)
G=0.353 (352/998, GoNL)
G=0.351 (277/790, PRJEB37584)
G=0.382 (229/600, NorthernSweden)
G=0.292 (132/452, SGDP_PRJ)
G=0.375 (114/304, HapMap)
G=0.282 (61/216, Qatari)
A=0.449 (97/216, Vietnamese)
G=0.27 (12/44, Siberian)
G=0.25 (10/40, GENOME_DK)
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: 20231103111315
Population Group Sample Size Ref Allele Alt Allele Ref HMOZ Alt HMOZ HTRZ HWEP
Total Global 248204 G=0.337658 A=0.662342 0.117299 0.441983 0.440718 15
European Sub 216522 G=0.332811 A=0.667189 0.11185 0.446227 0.441923 2
African Sub 10562 G=0.23708 A=0.76292 0.058512 0.584359 0.357129 1
African Others Sub 400 G=0.240 A=0.760 0.055 0.575 0.37 0
African American Sub 10162 G=0.23696 A=0.76304 0.05865 0.584727 0.356623 1
Asian Sub 3848 G=0.4296 A=0.5704 0.18815 0.329002 0.482848 0
East Asian Sub 3116 G=0.3947 A=0.6053 0.151476 0.362003 0.486521 0
Other Asian Sub 732 G=0.578 A=0.422 0.344262 0.188525 0.467213 0
Latin American 1 Sub 1028 G=0.3502 A=0.6498 0.122568 0.422179 0.455253 0
Latin American 2 Sub 6552 G=0.5524 A=0.4476 0.302198 0.197497 0.500305 0
South Asian Sub 366 G=0.497 A=0.503 0.20765 0.213115 0.579235 3
Other Sub 9326 G=0.3677 A=0.6323 0.147116 0.411752 0.441132 7


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=0.327889 A=0.672111
Allele Frequency Aggregator Total Global 243168 G=0.338268 A=0.661732
Allele Frequency Aggregator European Sub 213428 G=0.332927 A=0.667073
Allele Frequency Aggregator African Sub 9420 G=0.2386 A=0.7614
Allele Frequency Aggregator Other Sub 8526 G=0.3681 A=0.6319
Allele Frequency Aggregator Latin American 2 Sub 6552 G=0.5524 A=0.4476
Allele Frequency Aggregator Asian Sub 3848 G=0.4296 A=0.5704
Allele Frequency Aggregator Latin American 1 Sub 1028 G=0.3502 A=0.6498
Allele Frequency Aggregator South Asian Sub 366 G=0.497 A=0.503
gnomAD - Genomes Global Study-wide 140022 G=0.319921 A=0.680079
gnomAD - Genomes European Sub 75836 G=0.33835 A=0.66165
gnomAD - Genomes African Sub 41958 G=0.23748 A=0.76252
gnomAD - Genomes American Sub 13636 G=0.44632 A=0.55368
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.3034 A=0.6966
gnomAD - Genomes East Asian Sub 3122 G=0.4302 A=0.5698
gnomAD - Genomes Other Sub 2148 G=0.3426 A=0.6574
The PAGE Study Global Study-wide 78700 G=0.35053 A=0.64947
The PAGE Study AfricanAmerican Sub 32514 G=0.23741 A=0.76259
The PAGE Study Mexican Sub 10810 G=0.53617 A=0.46383
The PAGE Study Asian Sub 8318 G=0.4362 A=0.5638
The PAGE Study PuertoRican Sub 7918 G=0.3654 A=0.6346
The PAGE Study NativeHawaiian Sub 4534 G=0.3240 A=0.6760
The PAGE Study Cuban Sub 4230 G=0.3641 A=0.6359
The PAGE Study Dominican Sub 3828 G=0.3218 A=0.6782
The PAGE Study CentralAmerican Sub 2450 G=0.5298 A=0.4702
The PAGE Study SouthAmerican Sub 1982 G=0.5222 A=0.4778
The PAGE Study NativeAmerican Sub 1260 G=0.4008 A=0.5992
The PAGE Study SouthAsian Sub 856 G=0.551 A=0.449
14KJPN JAPANESE Study-wide 28256 G=0.43541 A=0.56459
8.3KJPN JAPANESE Study-wide 16760 G=0.43735 A=0.56265
1000Genomes_30x Global Study-wide 6404 G=0.4012 A=0.5988
1000Genomes_30x African Sub 1786 G=0.2307 A=0.7693
1000Genomes_30x Europe Sub 1266 G=0.3333 A=0.6667
1000Genomes_30x South Asian Sub 1202 G=0.5707 A=0.4293
1000Genomes_30x East Asian Sub 1170 G=0.4615 A=0.5385
1000Genomes_30x American Sub 980 G=0.519 A=0.481
1000Genomes Global Study-wide 5008 G=0.4034 A=0.5966
1000Genomes African Sub 1322 G=0.2269 A=0.7731
1000Genomes East Asian Sub 1008 G=0.4683 A=0.5317
1000Genomes Europe Sub 1006 G=0.3320 A=0.6680
1000Genomes South Asian Sub 978 G=0.569 A=0.431
1000Genomes American Sub 694 G=0.516 A=0.484
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.3779 A=0.6221
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.3326 A=0.6674
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.3220 A=0.6780
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.3802 A=0.6198, C=0.0000
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.353 A=0.647
CNV burdens in cranial meningiomas Global Study-wide 790 G=0.351 A=0.649
CNV burdens in cranial meningiomas CRM Sub 790 G=0.351 A=0.649
Northern Sweden ACPOP Study-wide 600 G=0.382 A=0.618
SGDP_PRJ Global Study-wide 452 G=0.292 A=0.708
HapMap Global Study-wide 304 G=0.375 A=0.625
HapMap African Sub 112 G=0.196 A=0.804
HapMap American Sub 106 G=0.443 A=0.557
HapMap Asian Sub 86 G=0.52 A=0.48
Qatari Global Study-wide 216 G=0.282 A=0.718
A Vietnamese Genetic Variation Database Global Study-wide 216 G=0.551 A=0.449
Siberian Global Study-wide 44 G=0.27 A=0.73
The Danish reference pan genome Danish Study-wide 40 G=0.25 A=0.75
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 2 NC_000002.12:g.190713628G>A
GRCh38.p14 chr 2 NC_000002.12:g.190713628G>C
GRCh37.p13 chr 2 NC_000002.11:g.191578354G>A
GRCh37.p13 chr 2 NC_000002.11:g.191578354G>C
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 C
GRCh38.p14 chr 2 NC_000002.12:g.190713628= NC_000002.12:g.190713628G>A NC_000002.12:g.190713628G>C
GRCh37.p13 chr 2 NC_000002.11:g.191578354= NC_000002.11:g.191578354G>A NC_000002.11:g.191578354G>C
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#.

117 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss9938379 Jul 11, 2003 (116)
2 CSHL-HAPMAP ss20080429 Feb 27, 2004 (120)
3 SSAHASNP ss21626451 Apr 05, 2004 (121)
4 PERLEGEN ss24163868 Sep 20, 2004 (123)
5 ABI ss44139186 Mar 13, 2006 (126)
6 HGSV ss81128610 Dec 15, 2007 (130)
7 HGSV ss84294286 Dec 15, 2007 (130)
8 BCMHGSC_JDW ss91488054 Mar 24, 2008 (129)
9 HUMANGENOME_JCVI ss97109447 Feb 05, 2009 (130)
10 BGI ss106149837 Feb 05, 2009 (130)
11 1000GENOMES ss111435941 Jan 25, 2009 (130)
12 ILLUMINA-UK ss118018481 Feb 14, 2009 (130)
13 ENSEMBL ss132890647 Dec 01, 2009 (131)
14 ENSEMBL ss138600896 Dec 01, 2009 (131)
15 GMI ss158117539 Dec 01, 2009 (131)
16 ILLUMINA ss159553739 Dec 01, 2009 (131)
17 ILLUMINA ss160802271 Dec 01, 2009 (131)
18 COMPLETE_GENOMICS ss165138198 Jul 04, 2010 (132)
19 COMPLETE_GENOMICS ss165764671 Jul 04, 2010 (132)
20 COMPLETE_GENOMICS ss167500127 Jul 04, 2010 (132)
21 BUSHMAN ss201530519 Jul 04, 2010 (132)
22 BCM-HGSC-SUB ss205725566 Jul 04, 2010 (132)
23 1000GENOMES ss219722206 Jul 14, 2010 (132)
24 1000GENOMES ss231521928 Jul 14, 2010 (132)
25 1000GENOMES ss238998142 Jul 15, 2010 (132)
26 GMI ss276837826 May 04, 2012 (137)
27 GMI ss284509803 Apr 25, 2013 (138)
28 PJP ss292449100 May 09, 2011 (134)
29 ILLUMINA ss481331077 May 04, 2012 (137)
30 ILLUMINA ss481356406 May 04, 2012 (137)
31 ILLUMINA ss482337064 Sep 08, 2015 (146)
32 ILLUMINA ss485460692 May 04, 2012 (137)
33 ILLUMINA ss537383632 Sep 08, 2015 (146)
34 TISHKOFF ss556115273 Apr 25, 2013 (138)
35 SSMP ss649778049 Apr 25, 2013 (138)
36 ILLUMINA ss778949256 Sep 08, 2015 (146)
37 ILLUMINA ss783175816 Sep 08, 2015 (146)
38 ILLUMINA ss784131236 Sep 08, 2015 (146)
39 ILLUMINA ss832435408 Sep 08, 2015 (146)
40 ILLUMINA ss833064909 Jul 13, 2019 (153)
41 ILLUMINA ss834411081 Sep 08, 2015 (146)
42 EVA-GONL ss977781518 Aug 21, 2014 (142)
43 JMKIDD_LAB ss1069807394 Aug 21, 2014 (142)
44 1000GENOMES ss1300946447 Aug 21, 2014 (142)
45 DDI ss1428860046 Apr 01, 2015 (144)
46 EVA_GENOME_DK ss1579254276 Apr 01, 2015 (144)
47 EVA_DECODE ss1587227953 Apr 01, 2015 (144)
48 EVA_UK10K_ALSPAC ss1605425105 Apr 01, 2015 (144)
49 EVA_UK10K_TWINSUK ss1648419138 Apr 01, 2015 (144)
50 ILLUMINA ss1752330263 Sep 08, 2015 (146)
51 HAMMER_LAB ss1798100832 Sep 08, 2015 (146)
52 WEILL_CORNELL_DGM ss1921029897 Feb 12, 2016 (147)
53 ILLUMINA ss1946062061 Feb 12, 2016 (147)
54 ILLUMINA ss1958490674 Feb 12, 2016 (147)
55 GENOMED ss1968983823 Jul 19, 2016 (147)
56 JJLAB ss2021056138 Sep 14, 2016 (149)
57 USC_VALOUEV ss2149121240 Dec 20, 2016 (150)
58 HUMAN_LONGEVITY ss2237670033 Dec 20, 2016 (150)
59 SYSTEMSBIOZJU ss2625031155 Nov 08, 2017 (151)
60 ILLUMINA ss2633719711 Nov 08, 2017 (151)
61 GRF ss2703764094 Nov 08, 2017 (151)
62 ILLUMINA ss2710921157 Nov 08, 2017 (151)
63 GNOMAD ss2784307995 Nov 08, 2017 (151)
64 SWEGEN ss2991076919 Nov 08, 2017 (151)
65 ILLUMINA ss3022053240 Nov 08, 2017 (151)
66 BIOINF_KMB_FNS_UNIBA ss3024288900 Nov 08, 2017 (151)
67 CSHL ss3344666447 Nov 08, 2017 (151)
68 ILLUMINA ss3625772619 Oct 11, 2018 (152)
69 ILLUMINA ss3628249584 Oct 11, 2018 (152)
70 ILLUMINA ss3631680608 Oct 11, 2018 (152)
71 ILLUMINA ss3633229041 Oct 11, 2018 (152)
72 ILLUMINA ss3633941998 Oct 11, 2018 (152)
73 ILLUMINA ss3634804741 Oct 11, 2018 (152)
74 ILLUMINA ss3635627542 Oct 11, 2018 (152)
75 ILLUMINA ss3636494008 Oct 11, 2018 (152)
76 ILLUMINA ss3637379551 Oct 11, 2018 (152)
77 ILLUMINA ss3640512040 Oct 11, 2018 (152)
78 ILLUMINA ss3644764725 Oct 11, 2018 (152)
79 URBANLAB ss3647236292 Oct 11, 2018 (152)
80 ILLUMINA ss3652500926 Oct 11, 2018 (152)
81 EGCUT_WGS ss3658959611 Jul 13, 2019 (153)
82 EVA_DECODE ss3705680179 Jul 13, 2019 (153)
83 ILLUMINA ss3725857558 Jul 13, 2019 (153)
84 ACPOP ss3729223268 Jul 13, 2019 (153)
85 ILLUMINA ss3744188199 Jul 13, 2019 (153)
86 ILLUMINA ss3745104575 Jul 13, 2019 (153)
87 EVA ss3757878568 Jul 13, 2019 (153)
88 PAGE_CC ss3770974318 Jul 13, 2019 (153)
89 ILLUMINA ss3772601126 Jul 13, 2019 (153)
90 PACBIO ss3784103379 Jul 13, 2019 (153)
91 PACBIO ss3789649425 Jul 13, 2019 (153)
92 PACBIO ss3794522555 Jul 13, 2019 (153)
93 KHV_HUMAN_GENOMES ss3802236689 Jul 13, 2019 (153)
94 EVA ss3827419672 Apr 25, 2020 (154)
95 EVA ss3837129394 Apr 25, 2020 (154)
96 EVA ss3842550127 Apr 25, 2020 (154)
97 SGDP_PRJ ss3854240037 Apr 25, 2020 (154)
98 KRGDB ss3899908134 Apr 25, 2020 (154)
99 EVA ss3984495501 Apr 26, 2021 (155)
100 EVA ss4017040750 Apr 26, 2021 (155)
101 TOPMED ss4538374037 Apr 26, 2021 (155)
102 TOMMO_GENOMICS ss5155702262 Apr 26, 2021 (155)
103 1000G_HIGH_COVERAGE ss5251419576 Oct 13, 2022 (156)
104 EVA ss5314796860 Oct 13, 2022 (156)
105 EVA ss5334917942 Oct 13, 2022 (156)
106 HUGCELL_USP ss5451096615 Oct 13, 2022 (156)
107 EVA ss5506738664 Oct 13, 2022 (156)
108 1000G_HIGH_COVERAGE ss5528446926 Oct 13, 2022 (156)
109 SANFORD_IMAGENETICS ss5630609698 Oct 13, 2022 (156)
110 TOMMO_GENOMICS ss5686352044 Oct 13, 2022 (156)
111 EVA ss5799555904 Oct 13, 2022 (156)
112 YY_MCH ss5803078739 Oct 13, 2022 (156)
113 EVA ss5821356405 Oct 13, 2022 (156)
114 EVA ss5847896857 Oct 13, 2022 (156)
115 EVA ss5852885806 Oct 13, 2022 (156)
116 EVA ss5934003564 Oct 13, 2022 (156)
117 EVA ss5956851435 Oct 13, 2022 (156)
118 1000Genomes NC_000002.11 - 191578354 Oct 11, 2018 (152)
119 1000Genomes_30x NC_000002.12 - 190713628 Oct 13, 2022 (156)
120 The Avon Longitudinal Study of Parents and Children NC_000002.11 - 191578354 Oct 11, 2018 (152)
121 Genetic variation in the Estonian population NC_000002.11 - 191578354 Oct 11, 2018 (152)
122 The Danish reference pan genome NC_000002.11 - 191578354 Apr 25, 2020 (154)
123 gnomAD - Genomes NC_000002.12 - 190713628 Apr 26, 2021 (155)
124 Genome of the Netherlands Release 5 NC_000002.11 - 191578354 Apr 25, 2020 (154)
125 HapMap NC_000002.12 - 190713628 Apr 25, 2020 (154)
126 KOREAN population from KRGDB NC_000002.11 - 191578354 Apr 25, 2020 (154)
127 Northern Sweden NC_000002.11 - 191578354 Jul 13, 2019 (153)
128 The PAGE Study NC_000002.12 - 190713628 Jul 13, 2019 (153)
129 CNV burdens in cranial meningiomas NC_000002.11 - 191578354 Apr 26, 2021 (155)
130 Qatari NC_000002.11 - 191578354 Apr 25, 2020 (154)
131 SGDP_PRJ NC_000002.11 - 191578354 Apr 25, 2020 (154)
132 Siberian NC_000002.11 - 191578354 Apr 25, 2020 (154)
133 8.3KJPN NC_000002.11 - 191578354 Apr 26, 2021 (155)
134 14KJPN NC_000002.12 - 190713628 Oct 13, 2022 (156)
135 TopMed NC_000002.12 - 190713628 Apr 26, 2021 (155)
136 UK 10K study - Twins NC_000002.11 - 191578354 Oct 11, 2018 (152)
137 A Vietnamese Genetic Variation Database NC_000002.11 - 191578354 Jul 13, 2019 (153)
138 ALFA NC_000002.12 - 190713628 Apr 26, 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)
rs59499930 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss81128610, ss84294286 NC_000002.9:191403859:G:A NC_000002.12:190713627:G:A (self)
ss91488054, ss111435941, ss118018481, ss165138198, ss165764671, ss167500127, ss201530519, ss205725566, ss276837826, ss284509803, ss292449100, ss481331077, ss1587227953 NC_000002.10:191286598:G:A NC_000002.12:190713627:G:A (self)
12024567, 6644779, 4697859, 5419215, 2918509, 7085528, 2508133, 44837, 3071827, 6257017, 1637594, 13671569, 6644779, 1448901, ss219722206, ss231521928, ss238998142, ss481356406, ss482337064, ss485460692, ss537383632, ss556115273, ss649778049, ss778949256, ss783175816, ss784131236, ss832435408, ss833064909, ss834411081, ss977781518, ss1069807394, ss1300946447, ss1428860046, ss1579254276, ss1605425105, ss1648419138, ss1752330263, ss1798100832, ss1921029897, ss1946062061, ss1958490674, ss1968983823, ss2021056138, ss2149121240, ss2625031155, ss2633719711, ss2703764094, ss2710921157, ss2784307995, ss2991076919, ss3022053240, ss3344666447, ss3625772619, ss3628249584, ss3631680608, ss3633229041, ss3633941998, ss3634804741, ss3635627542, ss3636494008, ss3637379551, ss3640512040, ss3644764725, ss3652500926, ss3658959611, ss3729223268, ss3744188199, ss3745104575, ss3757878568, ss3772601126, ss3784103379, ss3789649425, ss3794522555, ss3827419672, ss3837129394, ss3854240037, ss3899908134, ss3984495501, ss4017040750, ss5155702262, ss5314796860, ss5334917942, ss5506738664, ss5630609698, ss5799555904, ss5821356405, ss5847896857, ss5956851435 NC_000002.11:191578353:G:A NC_000002.12:190713627:G:A (self)
15972861, 85702422, 1976505, 195787, 20189148, 342196916, 7372589886, ss2237670033, ss3024288900, ss3647236292, ss3705680179, ss3725857558, ss3770974318, ss3802236689, ss3842550127, ss4538374037, ss5251419576, ss5451096615, ss5528446926, ss5686352044, ss5803078739, ss5852885806, ss5934003564 NC_000002.12:190713627:G:A NC_000002.12:190713627:G:A (self)
ss9938379 NT_005403.13:41737690:G:A NC_000002.12:190713627:G:A (self)
ss20080429, ss21626451 NT_005403.14:41787769:G:A NC_000002.12:190713627:G:A (self)
ss24163868, ss44139186, ss97109447, ss106149837, ss132890647, ss138600896, ss158117539, ss159553739, ss160802271 NT_005403.17:41787771:G:A NC_000002.12:190713627:G:A (self)
7085528, ss3899908134 NC_000002.11:191578353:G:C NC_000002.12:190713627:G:C (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 rs6721964

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.post820+afb47a3d