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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.

rs941986

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr6:125887883 (GRCh38.p13) 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
A>C / A>G / A>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.245857 (65076/264690, TOPMED)
G=0.247520 (34629/139904, GnomAD)
G=0.12129 (2085/17190, ALFA) (+ 16 more)
G=0.27613 (4628/16760, 8.3KJPN)
G=0.2428 (1216/5008, 1000G)
G=0.1663 (745/4480, Estonian)
G=0.1892 (729/3854, ALSPAC)
G=0.1775 (658/3708, TWINSUK)
G=0.2010 (589/2930, KOREAN)
G=0.1872 (343/1832, Korea1K)
G=0.2823 (502/1778, HapMap)
G=0.181 (181/998, GoNL)
G=0.195 (117/600, NorthernSweden)
G=0.264 (57/216, Qatari)
G=0.255 (55/216, Vietnamese)
A=0.394 (67/170, SGDP_PRJ)
G=0.23 (9/40, GENOME_DK)
A=0.50 (9/18, Siberian)
G=0.50 (9/18, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
NCOA7 : Intron Variant
Publications
0 citations
Genomic View
See rs on genome
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.p13 chr 6 NC_000006.12:g.125887883A>C
GRCh38.p13 chr 6 NC_000006.12:g.125887883A>G
GRCh38.p13 chr 6 NC_000006.12:g.125887883A>T
GRCh37.p13 chr 6 NC_000006.11:g.126209029A>C
GRCh37.p13 chr 6 NC_000006.11:g.126209029A>G
GRCh37.p13 chr 6 NC_000006.11:g.126209029A>T
Gene: NCOA7, nuclear receptor coactivator 7 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
NCOA7 transcript variant 2 NM_001122842.3:c.885-1089…

NM_001122842.3:c.885-1089A>C

N/A Intron Variant
NCOA7 transcript variant 3 NM_001199619.2:c.885-1056…

NM_001199619.2:c.885-1056A>C

N/A Intron Variant
NCOA7 transcript variant 4 NM_001199620.2:c.885-1056…

NM_001199620.2:c.885-1056A>C

N/A Intron Variant
NCOA7 transcript variant 5 NM_001199621.2:c.573-1089…

NM_001199621.2:c.573-1089A>C

N/A Intron Variant
NCOA7 transcript variant 1 NM_181782.5:c.885-1056A>C N/A Intron Variant
NCOA7 transcript variant 6 NM_001199622.2:c. N/A Genic Upstream Transcript Variant
NCOA7 transcript variant X3 XM_005266822.4:c.885-1056…

XM_005266822.4:c.885-1056A>C

N/A Intron Variant
NCOA7 transcript variant X4 XM_006715340.4:c.885-1056…

XM_006715340.4:c.885-1056A>C

N/A Intron Variant
NCOA7 transcript variant X1 XM_011535455.2:c.885-1056…

XM_011535455.2:c.885-1056A>C

N/A Intron Variant
NCOA7 transcript variant X5 XM_017010269.1:c.885-1056…

XM_017010269.1:c.885-1056A>C

N/A Intron Variant
NCOA7 transcript variant X6 XM_017010270.1:c.885-1089…

XM_017010270.1:c.885-1089A>C

N/A Intron Variant
NCOA7 transcript variant X7 XM_017010271.1:c.885-1089…

XM_017010271.1:c.885-1089A>C

N/A Intron Variant
NCOA7 transcript variant X9 XM_017010272.2:c.885-1089…

XM_017010272.2:c.885-1089A>C

N/A Intron Variant
NCOA7 transcript variant X10 XM_017010273.2:c.885-1089…

XM_017010273.2:c.885-1089A>C

N/A Intron Variant
NCOA7 transcript variant X11 XM_017010274.2:c.885-1089…

XM_017010274.2:c.885-1089A>C

N/A Intron Variant
NCOA7 transcript variant X2 XM_024446331.1:c.885-1056…

XM_024446331.1:c.885-1056A>C

N/A Intron Variant
NCOA7 transcript variant X8 XM_024446332.1:c.885-1089…

XM_024446332.1:c.885-1089A>C

N/A Intron Variant
NCOA7 transcript variant X12 XR_001743165.2:n. N/A Intron 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

ALFA Allele Frequency (New)
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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 17190 A=0.87871 C=0.00000, G=0.12129, T=0.00000
European Sub 13262 A=0.89149 C=0.00000, G=0.10851, T=0.00000
African Sub 2314 A=0.7736 C=0.0000, G=0.2264, T=0.0000
African Others Sub 66 A=0.82 C=0.00, G=0.18, T=0.00
African American Sub 2248 A=0.7722 C=0.0000, G=0.2278, T=0.0000
Asian Sub 72 A=0.99 C=0.00, G=0.01, T=0.00
East Asian Sub 54 A=0.98 C=0.00, G=0.02, T=0.00
Other Asian Sub 18 A=1.00 C=0.00, G=0.00, T=0.00
Latin American 1 Sub 114 A=0.965 C=0.000, G=0.035, T=0.000
Latin American 2 Sub 526 A=0.983 C=0.000, G=0.017, T=0.000
South Asian Sub 88 A=1.00 C=0.00, G=0.00, T=0.00
Other Sub 814 A=0.867 C=0.000, G=0.133, T=0.000


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 A=0.754143 G=0.245857
gnomAD - Genomes Global Study-wide 139904 A=0.752480 G=0.247520
gnomAD - Genomes European Sub 75788 A=0.80489 G=0.19511
gnomAD - Genomes African Sub 41918 A=0.61410 G=0.38590
gnomAD - Genomes American Sub 13606 A=0.85933 G=0.14067
gnomAD - Genomes Ashkenazi Jewish Sub 3320 A=0.8506 G=0.1494
gnomAD - Genomes East Asian Sub 3124 A=0.7548 G=0.2452
gnomAD - Genomes Other Sub 2148 A=0.7719 G=0.2281
8.3KJPN JAPANESE Study-wide 16760 A=0.72387 G=0.27613
1000Genomes Global Study-wide 5008 A=0.7572 G=0.2428
1000Genomes African Sub 1322 A=0.5635 G=0.4365
1000Genomes East Asian Sub 1008 A=0.7530 G=0.2470
1000Genomes Europe Sub 1006 A=0.8101 G=0.1899
1000Genomes South Asian Sub 978 A=0.891 G=0.109
1000Genomes American Sub 694 A=0.867 G=0.133
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.8337 G=0.1663
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.8108 G=0.1892
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.8225 G=0.1775
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.7990 G=0.2010
Korean Genome Project KOREAN Study-wide 1832 A=0.8128 G=0.1872
HapMap Global Study-wide 1778 A=0.7177 G=0.2823
HapMap African Sub 686 A=0.570 G=0.430
HapMap American Sub 666 A=0.812 G=0.188
HapMap Asian Sub 250 A=0.816 G=0.184
HapMap Europe Sub 176 A=0.795 G=0.205
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.819 G=0.181
Northern Sweden ACPOP Study-wide 600 A=0.805 G=0.195
Qatari Global Study-wide 216 A=0.736 G=0.264
A Vietnamese Genetic Variation Database Global Study-wide 216 A=0.745 G=0.255
SGDP_PRJ Global Study-wide 170 A=0.394 G=0.606
The Danish reference pan genome Danish Study-wide 40 A=0.78 G=0.23
Siberian Global Study-wide 18 A=0.50 G=0.50
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 A= C G T
GRCh38.p13 chr 6 NC_000006.12:g.125887883= NC_000006.12:g.125887883A>C NC_000006.12:g.125887883A>G NC_000006.12:g.125887883A>T
GRCh37.p13 chr 6 NC_000006.11:g.126209029= NC_000006.11:g.126209029A>C NC_000006.11:g.126209029A>G NC_000006.11:g.126209029A>T
NCOA7 transcript variant 2 NM_001122842.2:c.885-1089= NM_001122842.2:c.885-1089A>C NM_001122842.2:c.885-1089A>G NM_001122842.2:c.885-1089A>T
NCOA7 transcript variant 2 NM_001122842.3:c.885-1089= NM_001122842.3:c.885-1089A>C NM_001122842.3:c.885-1089A>G NM_001122842.3:c.885-1089A>T
NCOA7 transcript variant 3 NM_001199619.1:c.885-1056= NM_001199619.1:c.885-1056A>C NM_001199619.1:c.885-1056A>G NM_001199619.1:c.885-1056A>T
NCOA7 transcript variant 3 NM_001199619.2:c.885-1056= NM_001199619.2:c.885-1056A>C NM_001199619.2:c.885-1056A>G NM_001199619.2:c.885-1056A>T
NCOA7 transcript variant 4 NM_001199620.1:c.885-1056= NM_001199620.1:c.885-1056A>C NM_001199620.1:c.885-1056A>G NM_001199620.1:c.885-1056A>T
NCOA7 transcript variant 4 NM_001199620.2:c.885-1056= NM_001199620.2:c.885-1056A>C NM_001199620.2:c.885-1056A>G NM_001199620.2:c.885-1056A>T
NCOA7 transcript variant 5 NM_001199621.1:c.573-1089= NM_001199621.1:c.573-1089A>C NM_001199621.1:c.573-1089A>G NM_001199621.1:c.573-1089A>T
NCOA7 transcript variant 5 NM_001199621.2:c.573-1089= NM_001199621.2:c.573-1089A>C NM_001199621.2:c.573-1089A>G NM_001199621.2:c.573-1089A>T
NCOA7 transcript variant 1 NM_181782.4:c.885-1056= NM_181782.4:c.885-1056A>C NM_181782.4:c.885-1056A>G NM_181782.4:c.885-1056A>T
NCOA7 transcript variant 1 NM_181782.5:c.885-1056= NM_181782.5:c.885-1056A>C NM_181782.5:c.885-1056A>G NM_181782.5:c.885-1056A>T
NCOA7 transcript variant X1 XM_005266822.1:c.885-1056= XM_005266822.1:c.885-1056A>C XM_005266822.1:c.885-1056A>G XM_005266822.1:c.885-1056A>T
NCOA7 transcript variant X3 XM_005266822.4:c.885-1056= XM_005266822.4:c.885-1056A>C XM_005266822.4:c.885-1056A>G XM_005266822.4:c.885-1056A>T
NCOA7 transcript variant X2 XM_005266823.1:c.885-1056= XM_005266823.1:c.885-1056A>C XM_005266823.1:c.885-1056A>G XM_005266823.1:c.885-1056A>T
NCOA7 transcript variant X4 XM_006715340.4:c.885-1056= XM_006715340.4:c.885-1056A>C XM_006715340.4:c.885-1056A>G XM_006715340.4:c.885-1056A>T
NCOA7 transcript variant X1 XM_011535455.2:c.885-1056= XM_011535455.2:c.885-1056A>C XM_011535455.2:c.885-1056A>G XM_011535455.2:c.885-1056A>T
NCOA7 transcript variant X5 XM_017010269.1:c.885-1056= XM_017010269.1:c.885-1056A>C XM_017010269.1:c.885-1056A>G XM_017010269.1:c.885-1056A>T
NCOA7 transcript variant X6 XM_017010270.1:c.885-1089= XM_017010270.1:c.885-1089A>C XM_017010270.1:c.885-1089A>G XM_017010270.1:c.885-1089A>T
NCOA7 transcript variant X7 XM_017010271.1:c.885-1089= XM_017010271.1:c.885-1089A>C XM_017010271.1:c.885-1089A>G XM_017010271.1:c.885-1089A>T
NCOA7 transcript variant X9 XM_017010272.2:c.885-1089= XM_017010272.2:c.885-1089A>C XM_017010272.2:c.885-1089A>G XM_017010272.2:c.885-1089A>T
NCOA7 transcript variant X10 XM_017010273.2:c.885-1089= XM_017010273.2:c.885-1089A>C XM_017010273.2:c.885-1089A>G XM_017010273.2:c.885-1089A>T
NCOA7 transcript variant X11 XM_017010274.2:c.885-1089= XM_017010274.2:c.885-1089A>C XM_017010274.2:c.885-1089A>G XM_017010274.2:c.885-1089A>T
NCOA7 transcript variant X2 XM_024446331.1:c.885-1056= XM_024446331.1:c.885-1056A>C XM_024446331.1:c.885-1056A>G XM_024446331.1:c.885-1056A>T
NCOA7 transcript variant X8 XM_024446332.1:c.885-1089= XM_024446332.1:c.885-1089A>C XM_024446332.1:c.885-1089A>G XM_024446332.1:c.885-1089A>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#.

65 SubSNP, 18 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss1382878 Oct 05, 2000 (86)
2 SC_JCM ss6280746 Feb 20, 2003 (111)
3 BCM_SSAHASNP ss10332726 Jul 11, 2003 (116)
4 PERLEGEN ss23375828 Sep 20, 2004 (123)
5 ABI ss42657789 Mar 14, 2006 (126)
6 ILLUMINA ss65778563 Oct 16, 2006 (127)
7 ILLUMINA ss74855124 Dec 07, 2007 (129)
8 HGSV ss80192652 Dec 15, 2007 (130)
9 1000GENOMES ss115073243 Jan 25, 2009 (130)
10 ILLUMINA-UK ss116709343 Feb 14, 2009 (130)
11 KRIBB_YJKIM ss119374738 Dec 01, 2009 (131)
12 GMI ss157566419 Dec 01, 2009 (131)
13 COMPLETE_GENOMICS ss164489478 Jul 04, 2010 (132)
14 COMPLETE_GENOMICS ss167248300 Jul 04, 2010 (132)
15 ILLUMINA ss174840119 Jul 04, 2010 (132)
16 1000GENOMES ss222662503 Jul 14, 2010 (132)
17 1000GENOMES ss233675576 Jul 15, 2010 (132)
18 1000GENOMES ss240692672 Jul 15, 2010 (132)
19 GMI ss279015433 May 04, 2012 (137)
20 GMI ss285502052 Apr 25, 2013 (138)
21 ILLUMINA ss537597318 Sep 08, 2015 (146)
22 TISHKOFF ss559509524 Apr 25, 2013 (138)
23 SSMP ss653730061 Apr 25, 2013 (138)
24 EVA-GONL ss983477326 Aug 21, 2014 (142)
25 JMKIDD_LAB ss1074016936 Aug 21, 2014 (142)
26 1000GENOMES ss1322180874 Aug 21, 2014 (142)
27 DDI ss1430889735 Apr 01, 2015 (144)
28 EVA_GENOME_DK ss1581890097 Apr 01, 2015 (144)
29 EVA_DECODE ss1593044124 Apr 01, 2015 (144)
30 EVA_UK10K_ALSPAC ss1616646498 Apr 01, 2015 (144)
31 EVA_UK10K_TWINSUK ss1659640531 Apr 01, 2015 (144)
32 EVA_SVP ss1712898385 Apr 01, 2015 (144)
33 HAMMER_LAB ss1804661424 Sep 08, 2015 (146)
34 WEILL_CORNELL_DGM ss1926721715 Feb 12, 2016 (147)
35 JJLAB ss2024017143 Sep 14, 2016 (149)
36 USC_VALOUEV ss2152211548 Dec 20, 2016 (150)
37 HUMAN_LONGEVITY ss2288190150 Dec 20, 2016 (150)
38 TOPMED ss2456853521 Dec 20, 2016 (150)
39 SYSTEMSBIOZJU ss2626503942 Nov 08, 2017 (151)
40 GRF ss2707842459 Nov 08, 2017 (151)
41 SWEGEN ss2999917960 Nov 08, 2017 (151)
42 BIOINF_KMB_FNS_UNIBA ss3025803025 Nov 08, 2017 (151)
43 CSHL ss3347220547 Nov 08, 2017 (151)
44 TOPMED ss3511283437 Nov 08, 2017 (151)
45 ILLUMINA ss3629650253 Oct 12, 2018 (152)
46 ILLUMINA ss3638655806 Oct 12, 2018 (152)
47 ILLUMINA ss3643595035 Oct 12, 2018 (152)
48 EGCUT_WGS ss3667828792 Jul 13, 2019 (153)
49 EVA_DECODE ss3718234121 Jul 13, 2019 (153)
50 ACPOP ss3733965314 Jul 13, 2019 (153)
51 EVA ss3765644604 Jul 13, 2019 (153)
52 PACBIO ss3785615664 Jul 13, 2019 (153)
53 PACBIO ss3790944769 Jul 13, 2019 (153)
54 PACBIO ss3795824037 Jul 13, 2019 (153)
55 KHV_HUMAN_GENOMES ss3808801559 Jul 13, 2019 (153)
56 EVA ss3830183302 Apr 26, 2020 (154)
57 EVA ss3838578156 Apr 26, 2020 (154)
58 EVA ss3844028088 Apr 26, 2020 (154)
59 SGDP_PRJ ss3865661401 Apr 26, 2020 (154)
60 KRGDB ss3912612542 Apr 26, 2020 (154)
61 KOGIC ss3960041035 Apr 26, 2020 (154)
62 EVA ss4017298447 Apr 26, 2021 (155)
63 GNOMAD ss4151007301 Apr 26, 2021 (155)
64 TOPMED ss4721046275 Apr 26, 2021 (155)
65 TOMMO_GENOMICS ss5179832656 Apr 26, 2021 (155)
66 1000Genomes NC_000006.11 - 126209029 Oct 12, 2018 (152)
67 The Avon Longitudinal Study of Parents and Children NC_000006.11 - 126209029 Oct 12, 2018 (152)
68 Genetic variation in the Estonian population NC_000006.11 - 126209029 Oct 12, 2018 (152)
69 The Danish reference pan genome NC_000006.11 - 126209029 Apr 26, 2020 (154)
70 gnomAD - Genomes NC_000006.12 - 125887883 Apr 26, 2021 (155)
71 Genome of the Netherlands Release 5 NC_000006.11 - 126209029 Apr 26, 2020 (154)
72 HapMap NC_000006.12 - 125887883 Apr 26, 2020 (154)
73 KOREAN population from KRGDB NC_000006.11 - 126209029 Apr 26, 2020 (154)
74 Korean Genome Project NC_000006.12 - 125887883 Apr 26, 2020 (154)
75 Northern Sweden NC_000006.11 - 126209029 Jul 13, 2019 (153)
76 Qatari NC_000006.11 - 126209029 Apr 26, 2020 (154)
77 SGDP_PRJ NC_000006.11 - 126209029 Apr 26, 2020 (154)
78 Siberian NC_000006.11 - 126209029 Apr 26, 2020 (154)
79 8.3KJPN NC_000006.11 - 126209029 Apr 26, 2021 (155)
80 TopMed NC_000006.12 - 125887883 Apr 26, 2021 (155)
81 UK 10K study - Twins NC_000006.11 - 126209029 Oct 12, 2018 (152)
82 A Vietnamese Genetic Variation Database NC_000006.11 - 126209029 Jul 13, 2019 (153)
83 ALFA NC_000006.12 - 125887883 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)
rs59122077 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
7877956917 NC_000006.12:125887882:A:C NC_000006.12:125887882:A:C
ss80192652 NC_000006.9:126250721:A:G NC_000006.12:125887882:A:G (self)
ss115073243, ss116709343, ss164489478, ss167248300, ss279015433, ss285502052, ss1593044124, ss1712898385, ss3643595035 NC_000006.10:126250721:A:G NC_000006.12:125887882:A:G (self)
34046627, 18973357, 13567040, 8055036, 8452501, 19789936, 7250179, 8763645, 17678381, 4727902, 37801963, 18973357, 4225444, ss222662503, ss233675576, ss240692672, ss537597318, ss559509524, ss653730061, ss983477326, ss1074016936, ss1322180874, ss1430889735, ss1581890097, ss1616646498, ss1659640531, ss1804661424, ss1926721715, ss2024017143, ss2152211548, ss2456853521, ss2626503942, ss2707842459, ss2999917960, ss3347220547, ss3629650253, ss3638655806, ss3667828792, ss3733965314, ss3765644604, ss3785615664, ss3790944769, ss3795824037, ss3830183302, ss3838578156, ss3865661401, ss3912612542, ss4017298447, ss5179832656 NC_000006.11:126209028:A:G NC_000006.12:125887882:A:G (self)
240435323, 3243419, 16419036, 349286571, 558423833, 7877956917, ss2288190150, ss3025803025, ss3511283437, ss3718234121, ss3808801559, ss3844028088, ss3960041035, ss4151007301, ss4721046275 NC_000006.12:125887882:A:G NC_000006.12:125887882:A:G (self)
ss10332726 NT_025741.12:30313457:A:G NC_000006.12:125887882:A:G (self)
ss1382878, ss6280746, ss23375828, ss42657789, ss65778563, ss74855124, ss119374738, ss157566419, ss174840119 NT_025741.15:30378485:A:G NC_000006.12:125887882:A:G (self)
7877956917, ss2288190150 NC_000006.12:125887882:A:T NC_000006.12:125887882:A: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 rs941986

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.post596+ae089ad