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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.

rs2686221

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:241245729 (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>A / T>C
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.312524 (82722/264690, TOPMED)
T=0.314187 (43797/139398, GnomAD)
T=0.22314 (6305/28256, 14KJPN) (+ 14 more)
T=0.31101 (5875/18890, ALFA)
T=0.22422 (3758/16760, 8.3KJPN)
T=0.3278 (2099/6404, 1000G_30x)
T=0.3293 (1649/5008, 1000G)
T=0.3246 (1251/3854, ALSPAC)
T=0.3158 (1171/3708, TWINSUK)
T=0.3019 (884/2928, KOREAN)
T=0.2986 (547/1832, Korea1K)
T=0.314 (313/998, GoNL)
T=0.390 (234/600, NorthernSweden)
T=0.262 (125/478, SGDP_PRJ)
T=0.259 (56/216, Qatari)
T=0.29 (14/48, Siberian)
T=0.20 (8/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
RGS7 : Intron Variant
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 18890 T=0.31101 C=0.68899
European Sub 14286 T=0.31730 C=0.68270
African Sub 2946 T=0.2634 C=0.7366
African Others Sub 114 T=0.263 C=0.737
African American Sub 2832 T=0.2634 C=0.7366
Asian Sub 112 T=0.321 C=0.679
East Asian Sub 86 T=0.35 C=0.65
Other Asian Sub 26 T=0.23 C=0.77
Latin American 1 Sub 146 T=0.281 C=0.719
Latin American 2 Sub 610 T=0.357 C=0.643
South Asian Sub 98 T=0.40 C=0.60
Other Sub 692 T=0.335 C=0.665


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=0.312524 C=0.687476
gnomAD - Genomes Global Study-wide 139398 T=0.314187 C=0.685813
gnomAD - Genomes European Sub 75560 T=0.33142 C=0.66858
gnomAD - Genomes African Sub 41710 T=0.26689 C=0.73311
gnomAD - Genomes American Sub 13574 T=0.36076 C=0.63924
gnomAD - Genomes Ashkenazi Jewish Sub 3314 T=0.3129 C=0.6871
gnomAD - Genomes East Asian Sub 3106 T=0.3220 C=0.6780
gnomAD - Genomes Other Sub 2134 T=0.3229 C=0.6771
14KJPN JAPANESE Study-wide 28256 T=0.22314 C=0.77686
Allele Frequency Aggregator Total Global 18890 T=0.31101 C=0.68899
Allele Frequency Aggregator European Sub 14286 T=0.31730 C=0.68270
Allele Frequency Aggregator African Sub 2946 T=0.2634 C=0.7366
Allele Frequency Aggregator Other Sub 692 T=0.335 C=0.665
Allele Frequency Aggregator Latin American 2 Sub 610 T=0.357 C=0.643
Allele Frequency Aggregator Latin American 1 Sub 146 T=0.281 C=0.719
Allele Frequency Aggregator Asian Sub 112 T=0.321 C=0.679
Allele Frequency Aggregator South Asian Sub 98 T=0.40 C=0.60
8.3KJPN JAPANESE Study-wide 16760 T=0.22422 C=0.77578
1000Genomes_30x Global Study-wide 6404 T=0.3278 C=0.6722
1000Genomes_30x African Sub 1786 T=0.2727 C=0.7273
1000Genomes_30x Europe Sub 1266 T=0.3712 C=0.6288
1000Genomes_30x South Asian Sub 1202 T=0.3636 C=0.6364
1000Genomes_30x East Asian Sub 1170 T=0.3009 C=0.6991
1000Genomes_30x American Sub 980 T=0.360 C=0.640
1000Genomes Global Study-wide 5008 T=0.3293 C=0.6707
1000Genomes African Sub 1322 T=0.2693 C=0.7307
1000Genomes East Asian Sub 1008 T=0.2877 C=0.7123
1000Genomes Europe Sub 1006 T=0.3857 C=0.6143
1000Genomes South Asian Sub 978 T=0.367 C=0.633
1000Genomes American Sub 694 T=0.369 C=0.631
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.3246 C=0.6754
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.3158 C=0.6842
KOREAN population from KRGDB KOREAN Study-wide 2928 T=0.3019 A=0.0000, C=0.6981
Korean Genome Project KOREAN Study-wide 1832 T=0.2986 C=0.7014
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.314 C=0.686
Northern Sweden ACPOP Study-wide 600 T=0.390 C=0.610
SGDP_PRJ Global Study-wide 478 T=0.262 C=0.738
Qatari Global Study-wide 216 T=0.259 C=0.741
Siberian Global Study-wide 48 T=0.29 C=0.71
The Danish reference pan genome Danish Study-wide 40 T=0.20 C=0.80
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.241245729T>A
GRCh38.p14 chr 1 NC_000001.11:g.241245729T>C
GRCh37.p13 chr 1 NC_000001.10:g.241409029T>A
GRCh37.p13 chr 1 NC_000001.10:g.241409029T>C
Gene: RGS7, regulator of G protein signaling 7 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
RGS7 transcript variant 2 NM_001282773.2:c.78+10997…

NM_001282773.2:c.78+109970A>T

N/A Intron Variant
RGS7 transcript variant 3 NM_001282775.2:c.78+10997…

NM_001282775.2:c.78+109970A>T

N/A Intron Variant
RGS7 transcript variant 4 NM_001282778.2:c.78+10997…

NM_001282778.2:c.78+109970A>T

N/A Intron Variant
RGS7 transcript variant 5 NM_001350113.2:c.-1+10884…

NM_001350113.2:c.-1+108848A>T

N/A Intron Variant
RGS7 transcript variant 6 NM_001350114.2:c.-1+69835…

NM_001350114.2:c.-1+69835A>T

N/A Intron Variant
RGS7 transcript variant 7 NM_001350115.2:c.-1+10884…

NM_001350115.2:c.-1+108848A>T

N/A Intron Variant
RGS7 transcript variant 8 NM_001350116.1:c.-1+69835…

NM_001350116.1:c.-1+69835A>T

N/A Intron Variant
RGS7 transcript variant 9 NM_001364886.1:c.78+10997…

NM_001364886.1:c.78+109970A>T

N/A Intron Variant
RGS7 transcript variant 10 NM_001374806.1:c.78+10997…

NM_001374806.1:c.78+109970A>T

N/A Intron Variant
RGS7 transcript variant 11 NM_001374807.1:c.78+10997…

NM_001374807.1:c.78+109970A>T

N/A Intron Variant
RGS7 transcript variant 12 NM_001374808.1:c.-147+109…

NM_001374808.1:c.-147+109970A>T

N/A Intron Variant
RGS7 transcript variant 13 NM_001374809.1:c.-212+109…

NM_001374809.1:c.-212+109970A>T

N/A Intron Variant
RGS7 transcript variant 14 NM_001374810.1:c.-212+109…

NM_001374810.1:c.-212+109970A>T

N/A Intron Variant
RGS7 transcript variant 16 NM_001374811.1:c.78+10997…

NM_001374811.1:c.78+109970A>T

N/A Intron Variant
RGS7 transcript variant 15 NM_001374812.1:c.78+10997…

NM_001374812.1:c.78+109970A>T

N/A Intron Variant
RGS7 transcript variant 17 NM_001374813.1:c.-212+109…

NM_001374813.1:c.-212+109970A>T

N/A Intron Variant
RGS7 transcript variant 18 NM_001374814.1:c.78+10997…

NM_001374814.1:c.78+109970A>T

N/A Intron Variant
RGS7 transcript variant 19 NM_001374815.1:c.78+10997…

NM_001374815.1:c.78+109970A>T

N/A Intron Variant
RGS7 transcript variant 20 NM_001374816.1:c.78+10997…

NM_001374816.1:c.78+109970A>T

N/A Intron Variant
RGS7 transcript variant 1 NM_002924.6:c.78+109970A>T N/A Intron Variant
RGS7 transcript variant X2 XM_017002009.2:c. N/A Genic Upstream Transcript Variant
RGS7 transcript variant X1 XM_047426980.1:c. 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
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= A C
GRCh38.p14 chr 1 NC_000001.11:g.241245729= NC_000001.11:g.241245729T>A NC_000001.11:g.241245729T>C
GRCh37.p13 chr 1 NC_000001.10:g.241409029= NC_000001.10:g.241409029T>A NC_000001.10:g.241409029T>C
RGS7 transcript variant 2 NM_001282773.2:c.78+109970= NM_001282773.2:c.78+109970A>T NM_001282773.2:c.78+109970A>G
RGS7 transcript variant 3 NM_001282775.2:c.78+109970= NM_001282775.2:c.78+109970A>T NM_001282775.2:c.78+109970A>G
RGS7 transcript variant 4 NM_001282778.2:c.78+109970= NM_001282778.2:c.78+109970A>T NM_001282778.2:c.78+109970A>G
RGS7 transcript variant 5 NM_001350113.2:c.-1+108848= NM_001350113.2:c.-1+108848A>T NM_001350113.2:c.-1+108848A>G
RGS7 transcript variant 6 NM_001350114.2:c.-1+69835= NM_001350114.2:c.-1+69835A>T NM_001350114.2:c.-1+69835A>G
RGS7 transcript variant 7 NM_001350115.2:c.-1+108848= NM_001350115.2:c.-1+108848A>T NM_001350115.2:c.-1+108848A>G
RGS7 transcript variant 8 NM_001350116.1:c.-1+69835= NM_001350116.1:c.-1+69835A>T NM_001350116.1:c.-1+69835A>G
RGS7 transcript variant 9 NM_001364886.1:c.78+109970= NM_001364886.1:c.78+109970A>T NM_001364886.1:c.78+109970A>G
RGS7 transcript variant 10 NM_001374806.1:c.78+109970= NM_001374806.1:c.78+109970A>T NM_001374806.1:c.78+109970A>G
RGS7 transcript variant 11 NM_001374807.1:c.78+109970= NM_001374807.1:c.78+109970A>T NM_001374807.1:c.78+109970A>G
RGS7 transcript variant 12 NM_001374808.1:c.-147+109970= NM_001374808.1:c.-147+109970A>T NM_001374808.1:c.-147+109970A>G
RGS7 transcript variant 13 NM_001374809.1:c.-212+109970= NM_001374809.1:c.-212+109970A>T NM_001374809.1:c.-212+109970A>G
RGS7 transcript variant 14 NM_001374810.1:c.-212+109970= NM_001374810.1:c.-212+109970A>T NM_001374810.1:c.-212+109970A>G
RGS7 transcript variant 16 NM_001374811.1:c.78+109970= NM_001374811.1:c.78+109970A>T NM_001374811.1:c.78+109970A>G
RGS7 transcript variant 15 NM_001374812.1:c.78+109970= NM_001374812.1:c.78+109970A>T NM_001374812.1:c.78+109970A>G
RGS7 transcript variant 17 NM_001374813.1:c.-212+109970= NM_001374813.1:c.-212+109970A>T NM_001374813.1:c.-212+109970A>G
RGS7 transcript variant 18 NM_001374814.1:c.78+109970= NM_001374814.1:c.78+109970A>T NM_001374814.1:c.78+109970A>G
RGS7 transcript variant 19 NM_001374815.1:c.78+109970= NM_001374815.1:c.78+109970A>T NM_001374815.1:c.78+109970A>G
RGS7 transcript variant 20 NM_001374816.1:c.78+109970= NM_001374816.1:c.78+109970A>T NM_001374816.1:c.78+109970A>G
RGS7 transcript NM_002924.4:c.78+109970= NM_002924.4:c.78+109970A>T NM_002924.4:c.78+109970A>G
RGS7 transcript variant 1 NM_002924.6:c.78+109970= NM_002924.6:c.78+109970A>T NM_002924.6:c.78+109970A>G
RGS7 transcript variant X1 XM_005273218.1:c.78+109970= XM_005273218.1:c.78+109970A>T XM_005273218.1:c.78+109970A>G
RGS7 transcript variant X2 XM_005273219.1:c.78+109970= XM_005273219.1:c.78+109970A>T XM_005273219.1:c.78+109970A>G
RGS7 transcript variant X3 XM_005273220.1:c.78+109970= XM_005273220.1:c.78+109970A>T XM_005273220.1:c.78+109970A>G
RGS7 transcript variant X5 XM_005273222.1:c.78+109970= XM_005273222.1:c.78+109970A>T XM_005273222.1:c.78+109970A>G
RGS7 transcript variant X6 XM_005273223.1:c.78+109970= XM_005273223.1:c.78+109970A>T XM_005273223.1:c.78+109970A>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#.

64 SubSNP, 17 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss3792270 Sep 28, 2001 (100)
2 SC_SNP ss13017658 Dec 05, 2003 (126)
3 ABI ss41302721 Mar 10, 2006 (126)
4 HGSV ss78045084 Dec 07, 2007 (129)
5 BCMHGSC_JDW ss88032812 Mar 23, 2008 (129)
6 GMI ss156504487 Dec 01, 2009 (131)
7 COMPLETE_GENOMICS ss165543021 Jul 04, 2010 (132)
8 COMPLETE_GENOMICS ss165936052 Jul 04, 2010 (132)
9 COMPLETE_GENOMICS ss167582450 Jul 04, 2010 (132)
10 BUSHMAN ss199840573 Jul 04, 2010 (132)
11 BCM-HGSC-SUB ss205508263 Jul 04, 2010 (132)
12 GMI ss276289859 May 04, 2012 (137)
13 GMI ss284260923 Apr 25, 2013 (138)
14 1000GENOMES ss329331801 May 09, 2011 (134)
15 TISHKOFF ss555255030 Apr 25, 2013 (138)
16 SSMP ss648829115 Apr 25, 2013 (138)
17 EVA-GONL ss976333195 Aug 21, 2014 (142)
18 JMKIDD_LAB ss1068744656 Aug 21, 2014 (142)
19 1000GENOMES ss1295344402 Aug 21, 2014 (142)
20 DDI ss1426168077 Apr 01, 2015 (144)
21 EVA_GENOME_DK ss1574800512 Apr 01, 2015 (144)
22 EVA_DECODE ss1585737454 Apr 01, 2015 (144)
23 EVA_UK10K_ALSPAC ss1602512732 Apr 01, 2015 (144)
24 EVA_UK10K_TWINSUK ss1645506765 Apr 01, 2015 (144)
25 HAMMER_LAB ss1796000981 Sep 08, 2015 (146)
26 WEILL_CORNELL_DGM ss1919554995 Feb 12, 2016 (147)
27 JJLAB ss2020305141 Sep 14, 2016 (149)
28 USC_VALOUEV ss2148343144 Dec 20, 2016 (150)
29 HUMAN_LONGEVITY ss2171515207 Dec 20, 2016 (150)
30 SYSTEMSBIOZJU ss2624665927 Nov 08, 2017 (151)
31 GRF ss2698346815 Nov 08, 2017 (151)
32 GNOMAD ss2768163656 Nov 08, 2017 (151)
33 SWEGEN ss2988740075 Nov 08, 2017 (151)
34 BIOINF_KMB_FNS_UNIBA ss3023914993 Nov 08, 2017 (151)
35 CSHL ss3343997338 Nov 08, 2017 (151)
36 URBANLAB ss3646927264 Oct 11, 2018 (152)
37 EVA_DECODE ss3688979899 Jul 12, 2019 (153)
38 ACPOP ss3728020610 Jul 12, 2019 (153)
39 EVA ss3747555721 Jul 12, 2019 (153)
40 PACBIO ss3783737498 Jul 12, 2019 (153)
41 PACBIO ss3789342272 Jul 12, 2019 (153)
42 PACBIO ss3794214731 Jul 12, 2019 (153)
43 KHV_HUMAN_GENOMES ss3800559378 Jul 12, 2019 (153)
44 EVA ss3826739096 Apr 25, 2020 (154)
45 EVA ss3836772313 Apr 25, 2020 (154)
46 EVA ss3842185272 Apr 25, 2020 (154)
47 SGDP_PRJ ss3851266100 Apr 25, 2020 (154)
48 KRGDB ss3896626496 Apr 25, 2020 (154)
49 KOGIC ss3946849489 Apr 25, 2020 (154)
50 TOPMED ss4489556606 Apr 27, 2021 (155)
51 TOMMO_GENOMICS ss5149225986 Apr 27, 2021 (155)
52 1000G_HIGH_COVERAGE ss5246406264 Oct 17, 2022 (156)
53 EVA ss5325899009 Oct 17, 2022 (156)
54 HUGCELL_USP ss5446785522 Oct 17, 2022 (156)
55 EVA ss5506250142 Oct 17, 2022 (156)
56 1000G_HIGH_COVERAGE ss5520806556 Oct 17, 2022 (156)
57 SANFORD_IMAGENETICS ss5627797425 Oct 17, 2022 (156)
58 TOMMO_GENOMICS ss5677215714 Oct 17, 2022 (156)
59 YY_MCH ss5801797144 Oct 17, 2022 (156)
60 EVA ss5833511730 Oct 17, 2022 (156)
61 EVA ss5849366648 Oct 17, 2022 (156)
62 EVA ss5912674631 Oct 17, 2022 (156)
63 EVA ss5939647941 Oct 17, 2022 (156)
64 EVA ss5980026801 Oct 17, 2022 (156)
65 1000Genomes NC_000001.10 - 241409029 Oct 11, 2018 (152)
66 1000Genomes_30x NC_000001.11 - 241245729 Oct 17, 2022 (156)
67 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 241409029 Oct 11, 2018 (152)
68 The Danish reference pan genome NC_000001.10 - 241409029 Apr 25, 2020 (154)
69 gnomAD - Genomes NC_000001.11 - 241245729 Apr 27, 2021 (155)
70 Genome of the Netherlands Release 5 NC_000001.10 - 241409029 Apr 25, 2020 (154)
71 KOREAN population from KRGDB NC_000001.10 - 241409029 Apr 25, 2020 (154)
72 Korean Genome Project NC_000001.11 - 241245729 Apr 25, 2020 (154)
73 Northern Sweden NC_000001.10 - 241409029 Jul 12, 2019 (153)
74 Qatari NC_000001.10 - 241409029 Apr 25, 2020 (154)
75 SGDP_PRJ NC_000001.10 - 241409029 Apr 25, 2020 (154)
76 Siberian NC_000001.10 - 241409029 Apr 25, 2020 (154)
77 8.3KJPN NC_000001.10 - 241409029 Apr 27, 2021 (155)
78 14KJPN NC_000001.11 - 241245729 Oct 17, 2022 (156)
79 TopMed NC_000001.11 - 241245729 Apr 27, 2021 (155)
80 UK 10K study - Twins NC_000001.10 - 241409029 Oct 11, 2018 (152)
81 ALFA NC_000001.11 - 241245729 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)
rs9428867 Mar 10, 2006 (126)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
3803890, ss3896626496 NC_000001.10:241409028:T:A NC_000001.11:241245728:T:A (self)
ss78045084 NC_000001.8:237735069:T:C NC_000001.11:241245728:T:C (self)
ss88032812, ss165543021, ss165936052, ss167582450, ss199840573, ss205508263, ss276289859, ss284260923, ss1585737454 NC_000001.9:239475651:T:C NC_000001.11:241245728:T:C (self)
6225044, 3449536, 1961365, 1511221, 3803890, 1305475, 1596925, 3283080, 859498, 7195293, 3449536, ss329331801, ss555255030, ss648829115, ss976333195, ss1068744656, ss1295344402, ss1426168077, ss1574800512, ss1602512732, ss1645506765, ss1796000981, ss1919554995, ss2020305141, ss2148343144, ss2624665927, ss2698346815, ss2768163656, ss2988740075, ss3343997338, ss3728020610, ss3747555721, ss3783737498, ss3789342272, ss3794214731, ss3826739096, ss3836772313, ss3851266100, ss3896626496, ss5149225986, ss5325899009, ss5506250142, ss5627797425, ss5833511730, ss5939647941, ss5980026801 NC_000001.10:241409028:T:C NC_000001.11:241245728:T:C (self)
8332491, 44536237, 3227490, 11052818, 53162941, 9070458981, ss2171515207, ss3023914993, ss3646927264, ss3688979899, ss3800559378, ss3842185272, ss3946849489, ss4489556606, ss5246406264, ss5446785522, ss5520806556, ss5677215714, ss5801797144, ss5849366648, ss5912674631 NC_000001.11:241245728:T:C NC_000001.11:241245728:T:C (self)
ss13017658 NT_004836.14:6152387:T:C NC_000001.11:241245728:T:C (self)
ss3792270, ss41302721, ss156504487 NT_167186.1:34926807:T:C NC_000001.11:241245728:T:C (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs2686221

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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
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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