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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.

rs918921

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr15:94597545 (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>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.456232 (120760/264690, TOPMED)
A=0.425146 (100627/236688, ALFA)
A=0.445326 (62294/139884, GnomAD) (+ 20 more)
A=0.49221 (38738/78702, PAGE_STUDY)
G=0.40838 (11540/28258, 14KJPN)
G=0.40489 (6786/16760, 8.3KJPN)
G=0.4733 (3031/6404, 1000G_30x)
G=0.4722 (2365/5008, 1000G)
A=0.3953 (1771/4480, Estonian)
A=0.4193 (1616/3854, ALSPAC)
A=0.4369 (1620/3708, TWINSUK)
G=0.3845 (1125/2926, KOREAN)
G=0.3859 (707/1832, Korea1K)
A=0.446 (445/998, GoNL)
G=0.363 (287/790, PRJEB37584)
A=0.402 (241/600, NorthernSweden)
G=0.286 (127/444, SGDP_PRJ)
A=0.457 (150/328, HapMap)
G=0.444 (96/216, Qatari)
G=0.421 (90/214, Vietnamese)
G=0.50 (20/40, GENOME_DK)
A=0.50 (20/40, GENOME_DK)
G=0.41 (13/32, Siberian)
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 241724 G=0.574668 A=0.425332, T=0.000000
European Sub 215660 G=0.581216 A=0.418784, T=0.000000
African Sub 5980 G=0.5968 A=0.4032, T=0.0000
African Others Sub 240 G=0.571 A=0.429, T=0.000
African American Sub 5740 G=0.5979 A=0.4021, T=0.0000
Asian Sub 3762 G=0.3825 A=0.6175, T=0.0000
East Asian Sub 3050 G=0.4007 A=0.5993, T=0.0000
Other Asian Sub 712 G=0.305 A=0.695, T=0.000
Latin American 1 Sub 932 G=0.549 A=0.451, T=0.000
Latin American 2 Sub 6140 G=0.5292 A=0.4708, T=0.0000
South Asian Sub 278 G=0.313 A=0.687, T=0.000
Other Sub 8972 G=0.5250 A=0.4750, T=0.0000


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=0.543768 A=0.456232
Allele Frequency Aggregator Total Global 236688 G=0.574854 A=0.425146, T=0.000000
Allele Frequency Aggregator European Sub 212566 G=0.581142 A=0.418858, T=0.000000
Allele Frequency Aggregator Other Sub 8172 G=0.5257 A=0.4743, T=0.0000
Allele Frequency Aggregator Latin American 2 Sub 6140 G=0.5292 A=0.4708, T=0.0000
Allele Frequency Aggregator African Sub 4838 G=0.6091 A=0.3909, T=0.0000
Allele Frequency Aggregator Asian Sub 3762 G=0.3825 A=0.6175, T=0.0000
Allele Frequency Aggregator Latin American 1 Sub 932 G=0.549 A=0.451, T=0.000
Allele Frequency Aggregator South Asian Sub 278 G=0.313 A=0.687, T=0.000
gnomAD - Genomes Global Study-wide 139884 G=0.554674 A=0.445326
gnomAD - Genomes European Sub 75778 G=0.58275 A=0.41725
gnomAD - Genomes African Sub 41890 G=0.52662 A=0.47338
gnomAD - Genomes American Sub 13632 G=0.52634 A=0.47366
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.5379 A=0.4621
gnomAD - Genomes East Asian Sub 3116 G=0.3979 A=0.6021
gnomAD - Genomes Other Sub 2146 G=0.5443 A=0.4557
The PAGE Study Global Study-wide 78702 G=0.50779 A=0.49221
The PAGE Study AfricanAmerican Sub 32516 G=0.52774 A=0.47226
The PAGE Study Mexican Sub 10810 G=0.50259 A=0.49741
The PAGE Study Asian Sub 8318 G=0.4122 A=0.5878
The PAGE Study PuertoRican Sub 7918 G=0.5450 A=0.4550
The PAGE Study NativeHawaiian Sub 4534 G=0.4643 A=0.5357
The PAGE Study Cuban Sub 4230 G=0.5322 A=0.4678
The PAGE Study Dominican Sub 3828 G=0.5253 A=0.4747
The PAGE Study CentralAmerican Sub 2450 G=0.5249 A=0.4751
The PAGE Study SouthAmerican Sub 1982 G=0.5257 A=0.4743
The PAGE Study NativeAmerican Sub 1260 G=0.5167 A=0.4833
The PAGE Study SouthAsian Sub 856 G=0.328 A=0.672
14KJPN JAPANESE Study-wide 28258 G=0.40838 A=0.59162
8.3KJPN JAPANESE Study-wide 16760 G=0.40489 A=0.59511
1000Genomes_30x Global Study-wide 6404 G=0.4733 A=0.5267
1000Genomes_30x African Sub 1786 G=0.5118 A=0.4882
1000Genomes_30x Europe Sub 1266 G=0.5979 A=0.4021
1000Genomes_30x South Asian Sub 1202 G=0.2770 A=0.7230
1000Genomes_30x East Asian Sub 1170 G=0.4410 A=0.5590
1000Genomes_30x American Sub 980 G=0.521 A=0.479
1000Genomes Global Study-wide 5008 G=0.4722 A=0.5278
1000Genomes African Sub 1322 G=0.5219 A=0.4781
1000Genomes East Asian Sub 1008 G=0.4385 A=0.5615
1000Genomes Europe Sub 1006 G=0.5944 A=0.4056
1000Genomes South Asian Sub 978 G=0.278 A=0.722
1000Genomes American Sub 694 G=0.523 A=0.477
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.6047 A=0.3953
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.5807 A=0.4193
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.5631 A=0.4369
KOREAN population from KRGDB KOREAN Study-wide 2926 G=0.3845 A=0.6155
Korean Genome Project KOREAN Study-wide 1832 G=0.3859 A=0.6141
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.554 A=0.446
CNV burdens in cranial meningiomas Global Study-wide 790 G=0.363 A=0.637
CNV burdens in cranial meningiomas CRM Sub 790 G=0.363 A=0.637
Northern Sweden ACPOP Study-wide 600 G=0.598 A=0.402
SGDP_PRJ Global Study-wide 444 G=0.286 A=0.714
HapMap Global Study-wide 328 G=0.543 A=0.457
HapMap African Sub 120 G=0.483 A=0.517
HapMap American Sub 120 G=0.658 A=0.342
HapMap Asian Sub 88 G=0.47 A=0.53
Qatari Global Study-wide 216 G=0.444 A=0.556
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.421 A=0.579
The Danish reference pan genome Danish Study-wide 40 G=0.50 A=0.50
Siberian Global Study-wide 32 G=0.41 A=0.59
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 15 NC_000015.10:g.94597545G>A
GRCh38.p14 chr 15 NC_000015.10:g.94597545G>T
GRCh37.p13 chr 15 NC_000015.9:g.95140774G>A
GRCh37.p13 chr 15 NC_000015.9:g.95140774G>T
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 T
GRCh38.p14 chr 15 NC_000015.10:g.94597545= NC_000015.10:g.94597545G>A NC_000015.10:g.94597545G>T
GRCh37.p13 chr 15 NC_000015.9:g.95140774= NC_000015.9:g.95140774G>A NC_000015.9:g.95140774G>T
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#.

124 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss1354945 Oct 05, 2000 (86)
2 TSC-CSHL ss5469451 Oct 08, 2002 (108)
3 SC_JCM ss5653835 Feb 20, 2003 (111)
4 BCM_SSAHASNP ss14159773 Dec 05, 2003 (119)
5 CSHL-HAPMAP ss17540047 Feb 27, 2004 (120)
6 CSHL-HAPMAP ss20004543 Feb 27, 2004 (120)
7 SSAHASNP ss21292298 Apr 05, 2004 (121)
8 PERLEGEN ss24670954 Sep 20, 2004 (123)
9 ABI ss43767917 Mar 15, 2006 (126)
10 ILLUMINA ss65720839 Oct 13, 2006 (127)
11 HGSV ss77154538 Dec 06, 2007 (129)
12 BCMHGSC_JDW ss90261737 Mar 24, 2008 (129)
13 HUMANGENOME_JCVI ss96780816 Feb 04, 2009 (130)
14 BGI ss103264752 Dec 01, 2009 (131)
15 1000GENOMES ss109058579 Jan 23, 2009 (130)
16 1000GENOMES ss114588050 Jan 25, 2009 (130)
17 ILLUMINA-UK ss118339842 Feb 14, 2009 (130)
18 ILLUMINA ss120241560 Dec 01, 2009 (131)
19 ENSEMBL ss132440553 Dec 01, 2009 (131)
20 ENSEMBL ss136505757 Dec 01, 2009 (131)
21 GMI ss156891750 Dec 01, 2009 (131)
22 ILLUMINA ss160967850 Dec 01, 2009 (131)
23 COMPLETE_GENOMICS ss168530336 Jul 04, 2010 (132)
24 COMPLETE_GENOMICS ss170295900 Jul 04, 2010 (132)
25 BUSHMAN ss201218093 Jul 04, 2010 (132)
26 1000GENOMES ss227051832 Jul 14, 2010 (132)
27 1000GENOMES ss236889844 Jul 15, 2010 (132)
28 1000GENOMES ss243256130 Jul 15, 2010 (132)
29 ILLUMINA ss244259793 Jul 04, 2010 (132)
30 GMI ss282373864 May 04, 2012 (137)
31 PJP ss291780880 May 09, 2011 (134)
32 ILLUMINA ss481842496 May 04, 2012 (137)
33 ILLUMINA ss481875161 May 04, 2012 (137)
34 ILLUMINA ss482832286 Sep 08, 2015 (146)
35 ILLUMINA ss485715692 May 04, 2012 (137)
36 ILLUMINA ss537576657 Sep 08, 2015 (146)
37 TISHKOFF ss564669332 Apr 25, 2013 (138)
38 SSMP ss660412264 Apr 25, 2013 (138)
39 ILLUMINA ss779003996 Sep 08, 2015 (146)
40 ILLUMINA ss783303494 Sep 08, 2015 (146)
41 ILLUMINA ss784255696 Sep 08, 2015 (146)
42 ILLUMINA ss832564866 Sep 08, 2015 (146)
43 ILLUMINA ss834466396 Sep 08, 2015 (146)
44 EVA-GONL ss992108872 Aug 21, 2014 (142)
45 JMKIDD_LAB ss1080360276 Aug 21, 2014 (142)
46 1000GENOMES ss1354713308 Aug 21, 2014 (142)
47 DDI ss1427724757 Apr 01, 2015 (144)
48 EVA_GENOME_DK ss1577763567 Apr 01, 2015 (144)
49 EVA_UK10K_ALSPAC ss1633665706 Apr 01, 2015 (144)
50 EVA_UK10K_TWINSUK ss1676659739 Apr 01, 2015 (144)
51 EVA_DECODE ss1696139263 Apr 01, 2015 (144)
52 ILLUMINA ss1752179076 Sep 08, 2015 (146)
53 HAMMER_LAB ss1808341825 Sep 08, 2015 (146)
54 WEILL_CORNELL_DGM ss1935511936 Feb 12, 2016 (147)
55 ILLUMINA ss1946403260 Feb 12, 2016 (147)
56 ILLUMINA ss1959640621 Feb 12, 2016 (147)
57 GENOMED ss1968181130 Jul 19, 2016 (147)
58 JJLAB ss2028540559 Sep 14, 2016 (149)
59 USC_VALOUEV ss2156949810 Nov 08, 2017 (151)
60 HUMAN_LONGEVITY ss2209304465 Dec 20, 2016 (150)
61 SYSTEMSBIOZJU ss2628765609 Nov 08, 2017 (151)
62 ILLUMINA ss2633271248 Nov 08, 2017 (151)
63 GRF ss2701438580 Nov 08, 2017 (151)
64 ILLUMINA ss2710824266 Nov 08, 2017 (151)
65 GNOMAD ss2938469106 Nov 08, 2017 (151)
66 SWEGEN ss3013793483 Nov 08, 2017 (151)
67 ILLUMINA ss3021664206 Nov 08, 2017 (151)
68 BIOINF_KMB_FNS_UNIBA ss3028095075 Nov 08, 2017 (151)
69 CSHL ss3351255542 Nov 08, 2017 (151)
70 ILLUMINA ss3625681882 Oct 12, 2018 (152)
71 ILLUMINA ss3627437375 Oct 12, 2018 (152)
72 ILLUMINA ss3631261316 Oct 12, 2018 (152)
73 ILLUMINA ss3633108366 Oct 12, 2018 (152)
74 ILLUMINA ss3633813512 Oct 12, 2018 (152)
75 ILLUMINA ss3634622750 Oct 12, 2018 (152)
76 ILLUMINA ss3635502173 Oct 12, 2018 (152)
77 ILLUMINA ss3636313400 Oct 12, 2018 (152)
78 ILLUMINA ss3637253505 Oct 12, 2018 (152)
79 ILLUMINA ss3640330070 Oct 12, 2018 (152)
80 ILLUMINA ss3641065638 Oct 12, 2018 (152)
81 ILLUMINA ss3641361092 Oct 12, 2018 (152)
82 ILLUMINA ss3644656379 Oct 12, 2018 (152)
83 URBANLAB ss3650424612 Oct 12, 2018 (152)
84 ILLUMINA ss3652067285 Oct 12, 2018 (152)
85 EGCUT_WGS ss3680924145 Jul 13, 2019 (153)
86 EVA_DECODE ss3698510427 Jul 13, 2019 (153)
87 ILLUMINA ss3725527626 Jul 13, 2019 (153)
88 ACPOP ss3741191947 Jul 13, 2019 (153)
89 ILLUMINA ss3744135851 Jul 13, 2019 (153)
90 ILLUMINA ss3744923264 Jul 13, 2019 (153)
91 EVA ss3753476845 Jul 13, 2019 (153)
92 PAGE_CC ss3771852810 Jul 13, 2019 (153)
93 ILLUMINA ss3772421742 Jul 13, 2019 (153)
94 PACBIO ss3787934609 Jul 13, 2019 (153)
95 PACBIO ss3792932832 Jul 13, 2019 (153)
96 PACBIO ss3797817494 Jul 13, 2019 (153)
97 KHV_HUMAN_GENOMES ss3818779264 Jul 13, 2019 (153)
98 EVA ss3834390154 Apr 27, 2020 (154)
99 EVA ss3840798403 Apr 27, 2020 (154)
100 EVA ss3846288663 Apr 27, 2020 (154)
101 SGDP_PRJ ss3883578036 Apr 27, 2020 (154)
102 KRGDB ss3932834464 Apr 27, 2020 (154)
103 KOGIC ss3976789329 Apr 27, 2020 (154)
104 EVA ss3984706690 Apr 27, 2021 (155)
105 TOPMED ss5002273316 Apr 27, 2021 (155)
106 TOMMO_GENOMICS ss5217655249 Apr 27, 2021 (155)
107 1000G_HIGH_COVERAGE ss5299544410 Oct 16, 2022 (156)
108 EVA ss5315809433 Oct 16, 2022 (156)
109 EVA ss5421245997 Oct 16, 2022 (156)
110 HUGCELL_USP ss5493146443 Oct 16, 2022 (156)
111 EVA ss5511526588 Oct 16, 2022 (156)
112 1000G_HIGH_COVERAGE ss5601491648 Oct 16, 2022 (156)
113 SANFORD_IMAGENETICS ss5624369627 Oct 16, 2022 (156)
114 SANFORD_IMAGENETICS ss5658130431 Oct 16, 2022 (156)
115 TOMMO_GENOMICS ss5771902590 Oct 16, 2022 (156)
116 EVA ss5799947262 Oct 16, 2022 (156)
117 YY_MCH ss5815610510 Oct 16, 2022 (156)
118 EVA ss5828626929 Oct 16, 2022 (156)
119 EVA ss5847455040 Oct 16, 2022 (156)
120 EVA ss5847755751 Oct 16, 2022 (156)
121 EVA ss5851421362 Oct 16, 2022 (156)
122 EVA ss5877134436 Oct 16, 2022 (156)
123 EVA ss5949556440 Oct 16, 2022 (156)
124 EVA ss5979472138 Oct 16, 2022 (156)
125 1000Genomes NC_000015.9 - 95140774 Oct 12, 2018 (152)
126 1000Genomes_30x NC_000015.10 - 94597545 Oct 16, 2022 (156)
127 The Avon Longitudinal Study of Parents and Children NC_000015.9 - 95140774 Oct 12, 2018 (152)
128 Genetic variation in the Estonian population NC_000015.9 - 95140774 Oct 12, 2018 (152)
129 The Danish reference pan genome NC_000015.9 - 95140774 Apr 27, 2020 (154)
130 gnomAD - Genomes NC_000015.10 - 94597545 Apr 27, 2021 (155)
131 Genome of the Netherlands Release 5 NC_000015.9 - 95140774 Apr 27, 2020 (154)
132 HapMap NC_000015.10 - 94597545 Apr 27, 2020 (154)
133 KOREAN population from KRGDB NC_000015.9 - 95140774 Apr 27, 2020 (154)
134 Korean Genome Project NC_000015.10 - 94597545 Apr 27, 2020 (154)
135 Northern Sweden NC_000015.9 - 95140774 Jul 13, 2019 (153)
136 The PAGE Study NC_000015.10 - 94597545 Jul 13, 2019 (153)
137 CNV burdens in cranial meningiomas NC_000015.9 - 95140774 Apr 27, 2021 (155)
138 Qatari NC_000015.9 - 95140774 Apr 27, 2020 (154)
139 SGDP_PRJ NC_000015.9 - 95140774 Apr 27, 2020 (154)
140 Siberian NC_000015.9 - 95140774 Apr 27, 2020 (154)
141 8.3KJPN NC_000015.9 - 95140774 Apr 27, 2021 (155)
142 14KJPN NC_000015.10 - 94597545 Oct 16, 2022 (156)
143 TopMed NC_000015.10 - 94597545 Apr 27, 2021 (155)
144 UK 10K study - Twins NC_000015.9 - 95140774 Oct 12, 2018 (152)
145 A Vietnamese Genetic Variation Database NC_000015.9 - 95140774 Jul 13, 2019 (153)
146 ALFA NC_000015.10 - 94597545 Apr 27, 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)
rs17550621 Oct 08, 2004 (123)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss77154538, ss90261737, ss109058579, ss114588050, ss118339842, ss168530336, ss170295900, ss201218093, ss282373864, ss291780880, ss481842496, ss1696139263 NC_000015.8:92941777:G:A NC_000015.10:94597544:G:A (self)
67829570, 37670814, 26662393, 3982194, 16807443, 40011858, 14476812, 256218, 17553858, 35595016, 9466164, 75624556, 37670814, 8373635, ss227051832, ss236889844, ss243256130, ss481875161, ss482832286, ss485715692, ss537576657, ss564669332, ss660412264, ss779003996, ss783303494, ss784255696, ss832564866, ss834466396, ss992108872, ss1080360276, ss1354713308, ss1427724757, ss1577763567, ss1633665706, ss1676659739, ss1752179076, ss1808341825, ss1935511936, ss1946403260, ss1959640621, ss1968181130, ss2028540559, ss2156949810, ss2628765609, ss2633271248, ss2701438580, ss2710824266, ss2938469106, ss3013793483, ss3021664206, ss3351255542, ss3625681882, ss3627437375, ss3631261316, ss3633108366, ss3633813512, ss3634622750, ss3635502173, ss3636313400, ss3637253505, ss3640330070, ss3641065638, ss3641361092, ss3644656379, ss3652067285, ss3680924145, ss3741191947, ss3744135851, ss3744923264, ss3753476845, ss3772421742, ss3787934609, ss3792932832, ss3797817494, ss3834390154, ss3840798403, ss3883578036, ss3932834464, ss3984706690, ss5217655249, ss5315809433, ss5421245997, ss5511526588, ss5624369627, ss5658130431, ss5799947262, ss5828626929, ss5847455040, ss5847755751, ss5949556440, ss5979472138 NC_000015.9:95140773:G:A NC_000015.10:94597544:G:A (self)
89017583, 478160780, 1321568, 33167330, 1074279, 105739694, 217818976, 8279937243, ss2209304465, ss3028095075, ss3650424612, ss3698510427, ss3725527626, ss3771852810, ss3818779264, ss3846288663, ss3976789329, ss5002273316, ss5299544410, ss5493146443, ss5601491648, ss5771902590, ss5815610510, ss5851421362, ss5877134436 NC_000015.10:94597544:G:A NC_000015.10:94597544:G:A (self)
ss14159773, ss17540047, ss20004543, ss21292298 NT_010274.15:10106300:G:A NC_000015.10:94597544:G:A (self)
ss1354945, ss5469451, ss5653835, ss24670954, ss43767917, ss65720839, ss96780816, ss103264752, ss120241560, ss132440553, ss136505757, ss156891750, ss160967850, ss244259793 NT_010274.17:10106300:G:A NC_000015.10:94597544:G:A (self)
8279937243 NC_000015.10:94597544:G:T NC_000015.10:94597544:G:T (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 rs918921

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