Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

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.

rs9972931

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr17:33238758 (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
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.219010 (66569/303954, ALFA)
A=0.160089 (42374/264690, TOPMED)
A=0.167485 (23459/140066, GnomAD) (+ 21 more)
A=0.12252 (9642/78698, PAGE_STUDY)
A=0.19149 (5411/28258, 14KJPN)
A=0.19338 (3241/16760, 8.3KJPN)
A=0.1280 (820/6404, 1000G_30x)
A=0.1312 (657/5008, 1000G)
A=0.2045 (916/4480, Estonian)
A=0.2392 (922/3854, ALSPAC)
A=0.2279 (845/3708, TWINSUK)
A=0.2160 (633/2930, KOREAN)
A=0.1497 (312/2084, HGDP_Stanford)
A=0.2123 (389/1832, Korea1K)
A=0.1145 (204/1782, HapMap)
A=0.224 (224/998, GoNL)
A=0.213 (169/792, PRJEB37584)
A=0.237 (142/600, NorthernSweden)
A=0.171 (37/216, Qatari)
A=0.218 (45/206, Vietnamese)
G=0.449 (62/138, SGDP_PRJ)
A=0.24 (16/66, Ancient Sardinia)
A=0.15 (6/40, GENOME_DK)
G=0.46 (11/24, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ASIC2 : 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 308990 G=0.781517 A=0.218483
European Sub 272698 G=0.771623 A=0.228377
African Sub 9098 G=0.9532 A=0.0468
African Others Sub 372 G=0.997 A=0.003
African American Sub 8726 G=0.9513 A=0.0487
Asian Sub 3922 G=0.7909 A=0.2091
East Asian Sub 3176 G=0.7875 A=0.2125
Other Asian Sub 746 G=0.806 A=0.194
Latin American 1 Sub 1132 G=0.8101 A=0.1899
Latin American 2 Sub 7222 G=0.8343 A=0.1657
South Asian Sub 5222 G=0.8937 A=0.1063
Other Sub 9696 G=0.7919 A=0.2081


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
Allele Frequency Aggregator Total Global 303954 G=0.780990 A=0.219010
Allele Frequency Aggregator European Sub 269604 G=0.771695 A=0.228305
Allele Frequency Aggregator Other Sub 8896 G=0.7915 A=0.2085
Allele Frequency Aggregator African Sub 7956 G=0.9529 A=0.0471
Allele Frequency Aggregator Latin American 2 Sub 7222 G=0.8343 A=0.1657
Allele Frequency Aggregator South Asian Sub 5222 G=0.8937 A=0.1063
Allele Frequency Aggregator Asian Sub 3922 G=0.7909 A=0.2091
Allele Frequency Aggregator Latin American 1 Sub 1132 G=0.8101 A=0.1899
TopMed Global Study-wide 264690 G=0.839911 A=0.160089
gnomAD - Genomes Global Study-wide 140066 G=0.832515 A=0.167485
gnomAD - Genomes European Sub 75830 G=0.77017 A=0.22983
gnomAD - Genomes African Sub 41998 G=0.95733 A=0.04267
gnomAD - Genomes American Sub 13644 G=0.83018 A=0.16982
gnomAD - Genomes Ashkenazi Jewish Sub 3316 G=0.7434 A=0.2566
gnomAD - Genomes East Asian Sub 3126 G=0.7882 A=0.2118
gnomAD - Genomes Other Sub 2152 G=0.8099 A=0.1901
The PAGE Study Global Study-wide 78698 G=0.87748 A=0.12252
The PAGE Study AfricanAmerican Sub 32514 G=0.94901 A=0.05099
The PAGE Study Mexican Sub 10810 G=0.83099 A=0.16901
The PAGE Study Asian Sub 8318 G=0.7987 A=0.2013
The PAGE Study PuertoRican Sub 7918 G=0.8450 A=0.1550
The PAGE Study NativeHawaiian Sub 4532 G=0.7882 A=0.2118
The PAGE Study Cuban Sub 4230 G=0.7939 A=0.2061
The PAGE Study Dominican Sub 3828 G=0.8683 A=0.1317
The PAGE Study CentralAmerican Sub 2450 G=0.8816 A=0.1184
The PAGE Study SouthAmerican Sub 1982 G=0.8360 A=0.1640
The PAGE Study NativeAmerican Sub 1260 G=0.8325 A=0.1675
The PAGE Study SouthAsian Sub 856 G=0.890 A=0.110
14KJPN JAPANESE Study-wide 28258 G=0.80851 A=0.19149
8.3KJPN JAPANESE Study-wide 16760 G=0.80662 A=0.19338
1000Genomes_30x Global Study-wide 6404 G=0.8720 A=0.1280
1000Genomes_30x African Sub 1786 G=0.9910 A=0.0090
1000Genomes_30x Europe Sub 1266 G=0.7686 A=0.2314
1000Genomes_30x South Asian Sub 1202 G=0.9243 A=0.0757
1000Genomes_30x East Asian Sub 1170 G=0.8077 A=0.1923
1000Genomes_30x American Sub 980 G=0.801 A=0.199
1000Genomes Global Study-wide 5008 G=0.8688 A=0.1312
1000Genomes African Sub 1322 G=0.9894 A=0.0106
1000Genomes East Asian Sub 1008 G=0.8056 A=0.1944
1000Genomes Europe Sub 1006 G=0.7654 A=0.2346
1000Genomes South Asian Sub 978 G=0.921 A=0.079
1000Genomes American Sub 694 G=0.807 A=0.193
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.7955 A=0.2045
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.7608 A=0.2392
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.7721 A=0.2279
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.7840 A=0.2160
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.8503 A=0.1497
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.806 A=0.194
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.903 A=0.097
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.829 A=0.171
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.741 A=0.259
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.996 A=0.004
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.843 A=0.157
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.96 A=0.04
Korean Genome Project KOREAN Study-wide 1832 G=0.7877 A=0.2123
HapMap Global Study-wide 1782 G=0.8855 A=0.1145
HapMap American Sub 766 G=0.839 A=0.161
HapMap African Sub 586 G=0.990 A=0.010
HapMap Asian Sub 254 G=0.843 A=0.157
HapMap Europe Sub 176 G=0.801 A=0.199
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.776 A=0.224
CNV burdens in cranial meningiomas Global Study-wide 792 G=0.787 A=0.213
CNV burdens in cranial meningiomas CRM Sub 792 G=0.787 A=0.213
Northern Sweden ACPOP Study-wide 600 G=0.763 A=0.237
Qatari Global Study-wide 216 G=0.829 A=0.171
A Vietnamese Genetic Variation Database Global Study-wide 206 G=0.782 A=0.218
SGDP_PRJ Global Study-wide 138 G=0.449 A=0.551
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 66 G=0.76 A=0.24
The Danish reference pan genome Danish Study-wide 40 G=0.85 A=0.15
Siberian Global Study-wide 24 G=0.46 A=0.54
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 17 NC_000017.11:g.33238758G>A
GRCh37.p13 chr 17 NC_000017.10:g.31565776G>A
ASIC2 RefSeqGene NG_029763.1:g.923050C>T
Gene: ASIC2, acid sensing ion channel subunit 2 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ASIC2 transcript variant MDEG1 NM_001094.5:c.556-126691C…

NM_001094.5:c.556-126691C>T

N/A Intron Variant
ASIC2 transcript variant MDEG2 NM_183377.2:c.708+52650C>T 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
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
GRCh38.p14 chr 17 NC_000017.11:g.33238758= NC_000017.11:g.33238758G>A
GRCh37.p13 chr 17 NC_000017.10:g.31565776= NC_000017.10:g.31565776G>A
ASIC2 RefSeqGene NG_029763.1:g.923050= NG_029763.1:g.923050C>T
ASIC2 transcript variant MDEG1 NM_001094.4:c.556-126691= NM_001094.4:c.556-126691C>T
ASIC2 transcript variant MDEG1 NM_001094.5:c.556-126691= NM_001094.5:c.556-126691C>T
ASIC2 transcript variant MDEG2 NM_183377.1:c.708+52650= NM_183377.1:c.708+52650C>T
ASIC2 transcript variant MDEG2 NM_183377.2:c.708+52650= NM_183377.2:c.708+52650C>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#.

118 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 WUGSC_SSAHASNP ss13814857 Dec 05, 2003 (119)
2 SSAHASNP ss21382258 Apr 05, 2004 (121)
3 ABI ss40797234 Mar 14, 2006 (126)
4 ILLUMINA ss66856610 Dec 01, 2006 (127)
5 ILLUMINA ss67965981 Dec 01, 2006 (127)
6 ILLUMINA ss68072535 Dec 01, 2006 (127)
7 ILLUMINA ss71637407 May 17, 2007 (127)
8 ILLUMINA ss75906707 Dec 06, 2007 (129)
9 ILLUMINA ss79309528 Dec 16, 2007 (130)
10 KRIBB_YJKIM ss84883643 Dec 16, 2007 (130)
11 ILLUMINA ss98308034 May 27, 2008 (130)
12 ILLUMINA ss123070491 Dec 01, 2009 (131)
13 ENSEMBL ss132592990 Dec 01, 2009 (131)
14 ENSEMBL ss137044658 Dec 01, 2009 (131)
15 ILLUMINA ss154520285 Dec 01, 2009 (131)
16 ILLUMINA ss159694114 Dec 01, 2009 (131)
17 ILLUMINA ss161030082 Dec 01, 2009 (131)
18 COMPLETE_GENOMICS ss171323336 Jul 04, 2010 (132)
19 ILLUMINA ss172524205 Jul 04, 2010 (132)
20 ILLUMINA ss174940068 Jul 04, 2010 (132)
21 1000GENOMES ss237223390 Jul 15, 2010 (132)
22 1000GENOMES ss243526011 Jul 15, 2010 (132)
23 BL ss255590870 May 09, 2011 (134)
24 GMI ss282744704 May 04, 2012 (137)
25 PJP ss292039183 May 09, 2011 (134)
26 ILLUMINA ss482035022 May 04, 2012 (137)
27 ILLUMINA ss482069484 May 04, 2012 (137)
28 ILLUMINA ss483018293 Sep 08, 2015 (146)
29 ILLUMINA ss485811003 May 04, 2012 (137)
30 ILLUMINA ss537649924 Sep 08, 2015 (146)
31 SSMP ss661036922 Apr 25, 2013 (138)
32 ILLUMINA ss778653472 Sep 08, 2015 (146)
33 ILLUMINA ss783351360 Sep 08, 2015 (146)
34 ILLUMINA ss784302534 Sep 08, 2015 (146)
35 ILLUMINA ss825640046 Apr 01, 2015 (144)
36 ILLUMINA ss832613397 Sep 08, 2015 (146)
37 ILLUMINA ss833204766 Jul 13, 2019 (153)
38 ILLUMINA ss834111336 Sep 08, 2015 (146)
39 EVA-GONL ss993047108 Aug 21, 2014 (142)
40 JMKIDD_LAB ss1081017456 Aug 21, 2014 (142)
41 1000GENOMES ss1358407952 Aug 21, 2014 (142)
42 DDI ss1428017436 Apr 01, 2015 (144)
43 EVA_GENOME_DK ss1578133890 Apr 01, 2015 (144)
44 EVA_UK10K_ALSPAC ss1635527729 Apr 01, 2015 (144)
45 EVA_UK10K_TWINSUK ss1678521762 Apr 01, 2015 (144)
46 EVA_DECODE ss1697087859 Apr 01, 2015 (144)
47 EVA_SVP ss1713578031 Apr 01, 2015 (144)
48 ILLUMINA ss1752221138 Sep 08, 2015 (146)
49 WEILL_CORNELL_DGM ss1936505289 Feb 12, 2016 (147)
50 ILLUMINA ss1946440128 Feb 12, 2016 (147)
51 ILLUMINA ss1959739701 Feb 12, 2016 (147)
52 GENOMED ss1968377969 Jul 19, 2016 (147)
53 JJLAB ss2029031058 Sep 14, 2016 (149)
54 USC_VALOUEV ss2157496689 Dec 20, 2016 (150)
55 HUMAN_LONGEVITY ss2216360288 Dec 20, 2016 (150)
56 ILLUMINA ss2633388983 Nov 08, 2017 (151)
57 GRF ss2702056582 Nov 08, 2017 (151)
58 ILLUMINA ss2710847137 Nov 08, 2017 (151)
59 GNOMAD ss2949141610 Nov 08, 2017 (151)
60 SWEGEN ss3015429761 Nov 08, 2017 (151)
61 ILLUMINA ss3021771735 Nov 08, 2017 (151)
62 BIOINF_KMB_FNS_UNIBA ss3028335782 Nov 08, 2017 (151)
63 CSHL ss3351718878 Nov 08, 2017 (151)
64 ILLUMINA ss3625707735 Oct 12, 2018 (152)
65 ILLUMINA ss3627653679 Oct 12, 2018 (152)
66 ILLUMINA ss3631370644 Oct 12, 2018 (152)
67 ILLUMINA ss3633139397 Oct 12, 2018 (152)
68 ILLUMINA ss3633846764 Oct 12, 2018 (152)
69 ILLUMINA ss3634671233 Oct 12, 2018 (152)
70 ILLUMINA ss3635534588 Oct 12, 2018 (152)
71 ILLUMINA ss3636361236 Oct 12, 2018 (152)
72 ILLUMINA ss3637286112 Oct 12, 2018 (152)
73 ILLUMINA ss3638157003 Oct 12, 2018 (152)
74 ILLUMINA ss3639088483 Oct 12, 2018 (152)
75 ILLUMINA ss3639551126 Oct 12, 2018 (152)
76 ILLUMINA ss3640378548 Oct 12, 2018 (152)
77 ILLUMINA ss3641079682 Oct 12, 2018 (152)
78 ILLUMINA ss3641375163 Oct 12, 2018 (152)
79 ILLUMINA ss3643135902 Oct 12, 2018 (152)
80 ILLUMINA ss3644685591 Oct 12, 2018 (152)
81 URBANLAB ss3650639046 Oct 12, 2018 (152)
82 ILLUMINA ss3652185775 Oct 12, 2018 (152)
83 EGCUT_WGS ss3682328831 Jul 13, 2019 (153)
84 EVA_DECODE ss3700343518 Jul 13, 2019 (153)
85 ILLUMINA ss3725614505 Jul 13, 2019 (153)
86 ACPOP ss3741975349 Jul 13, 2019 (153)
87 ILLUMINA ss3744149207 Jul 13, 2019 (153)
88 ILLUMINA ss3744971545 Jul 13, 2019 (153)
89 EVA ss3754594633 Jul 13, 2019 (153)
90 PAGE_CC ss3771922100 Jul 13, 2019 (153)
91 ILLUMINA ss3772469473 Jul 13, 2019 (153)
92 KHV_HUMAN_GENOMES ss3819872654 Jul 13, 2019 (153)
93 EVA ss3834837317 Apr 27, 2020 (154)
94 EVA ss3841028277 Apr 27, 2020 (154)
95 EVA ss3846525234 Apr 27, 2020 (154)
96 HGDP ss3847562275 Apr 27, 2020 (154)
97 SGDP_PRJ ss3885617353 Apr 27, 2020 (154)
98 KRGDB ss3935278508 Apr 27, 2020 (154)
99 KOGIC ss3978750545 Apr 27, 2020 (154)
100 EVA ss3984722017 Apr 26, 2021 (155)
101 EVA ss3985787493 Apr 26, 2021 (155)
102 EVA ss4017763234 Apr 26, 2021 (155)
103 TOPMED ss5033844136 Apr 26, 2021 (155)
104 TOMMO_GENOMICS ss5222115173 Apr 26, 2021 (155)
105 1000G_HIGH_COVERAGE ss5302911995 Oct 16, 2022 (156)
106 EVA ss5315882097 Oct 16, 2022 (156)
107 EVA ss5427199311 Oct 16, 2022 (156)
108 HUGCELL_USP ss5495997997 Oct 16, 2022 (156)
109 EVA ss5511752012 Oct 16, 2022 (156)
110 1000G_HIGH_COVERAGE ss5606525088 Oct 16, 2022 (156)
111 SANFORD_IMAGENETICS ss5659980686 Oct 16, 2022 (156)
112 TOMMO_GENOMICS ss5778228658 Oct 16, 2022 (156)
113 EVA ss5799973803 Oct 16, 2022 (156)
114 YY_MCH ss5816491065 Oct 16, 2022 (156)
115 EVA ss5833898577 Oct 16, 2022 (156)
116 EVA ss5851785012 Oct 16, 2022 (156)
117 EVA ss5913717552 Oct 16, 2022 (156)
118 EVA ss5951376223 Oct 16, 2022 (156)
119 1000Genomes NC_000017.10 - 31565776 Oct 12, 2018 (152)
120 1000Genomes_30x NC_000017.11 - 33238758 Oct 16, 2022 (156)
121 The Avon Longitudinal Study of Parents and Children NC_000017.10 - 31565776 Oct 12, 2018 (152)
122 Genetic variation in the Estonian population NC_000017.10 - 31565776 Oct 12, 2018 (152)
123 The Danish reference pan genome NC_000017.10 - 31565776 Apr 27, 2020 (154)
124 gnomAD - Genomes NC_000017.11 - 33238758 Apr 26, 2021 (155)
125 Genome of the Netherlands Release 5 NC_000017.10 - 31565776 Apr 27, 2020 (154)
126 HGDP-CEPH-db Supplement 1 NC_000017.9 - 28589889 Apr 27, 2020 (154)
127 HapMap NC_000017.11 - 33238758 Apr 27, 2020 (154)
128 KOREAN population from KRGDB NC_000017.10 - 31565776 Apr 27, 2020 (154)
129 Korean Genome Project NC_000017.11 - 33238758 Apr 27, 2020 (154)
130 Northern Sweden NC_000017.10 - 31565776 Jul 13, 2019 (153)
131 The PAGE Study NC_000017.11 - 33238758 Jul 13, 2019 (153)
132 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000017.10 - 31565776 Apr 26, 2021 (155)
133 CNV burdens in cranial meningiomas NC_000017.10 - 31565776 Apr 26, 2021 (155)
134 Qatari NC_000017.10 - 31565776 Apr 27, 2020 (154)
135 SGDP_PRJ NC_000017.10 - 31565776 Apr 27, 2020 (154)
136 Siberian NC_000017.10 - 31565776 Apr 27, 2020 (154)
137 8.3KJPN NC_000017.10 - 31565776 Apr 26, 2021 (155)
138 14KJPN NC_000017.11 - 33238758 Oct 16, 2022 (156)
139 TopMed NC_000017.11 - 33238758 Apr 26, 2021 (155)
140 UK 10K study - Twins NC_000017.10 - 31565776 Oct 12, 2018 (152)
141 A Vietnamese Genetic Variation Database NC_000017.10 - 31565776 Jul 13, 2019 (153)
142 ALFA NC_000017.11 - 33238758 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)
rs61509265 May 27, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
240167, ss171323336, ss255590870, ss282744704, ss292039183, ss482035022, ss825640046, ss1697087859, ss1713578031, ss3639088483, ss3639551126, ss3643135902, ss3847562275 NC_000017.9:28589888:G:A NC_000017.11:33238757:G:A (self)
71640943, 39710123, 28067079, 4337081, 17702037, 42455902, 15260214, 1013420, 271562, 18547211, 37634333, 10013043, 80084480, 39710123, 8790580, ss237223390, ss243526011, ss482069484, ss483018293, ss485811003, ss537649924, ss661036922, ss778653472, ss783351360, ss784302534, ss832613397, ss833204766, ss834111336, ss993047108, ss1081017456, ss1358407952, ss1428017436, ss1578133890, ss1635527729, ss1678521762, ss1752221138, ss1936505289, ss1946440128, ss1959739701, ss1968377969, ss2029031058, ss2157496689, ss2633388983, ss2702056582, ss2710847137, ss2949141610, ss3015429761, ss3021771735, ss3351718878, ss3625707735, ss3627653679, ss3631370644, ss3633139397, ss3633846764, ss3634671233, ss3635534588, ss3636361236, ss3637286112, ss3638157003, ss3640378548, ss3641079682, ss3641375163, ss3644685591, ss3652185775, ss3682328831, ss3741975349, ss3744149207, ss3744971545, ss3754594633, ss3772469473, ss3834837317, ss3841028277, ss3885617353, ss3935278508, ss3984722017, ss3985787493, ss4017763234, ss5222115173, ss5315882097, ss5427199311, ss5511752012, ss5659980686, ss5799973803, ss5833898577, ss5951376223 NC_000017.10:31565775:G:A NC_000017.11:33238757:G:A (self)
94051023, 505411208, 1477850, 35128546, 1143569, 112065762, 249389798, 6753264212, ss2216360288, ss3028335782, ss3650639046, ss3700343518, ss3725614505, ss3771922100, ss3819872654, ss3846525234, ss3978750545, ss5033844136, ss5302911995, ss5495997997, ss5606525088, ss5778228658, ss5816491065, ss5851785012, ss5913717552 NC_000017.11:33238757:G:A NC_000017.11:33238757:G:A (self)
ss13814857, ss21382258 NT_010799.14:6302755:G:A NC_000017.11:33238757:G:A (self)
ss40797234, ss66856610, ss67965981, ss68072535, ss71637407, ss75906707, ss79309528, ss84883643, ss98308034, ss123070491, ss132592990, ss137044658, ss154520285, ss159694114, ss161030082, ss172524205, ss174940068 NT_010799.15:6302769:G:A NC_000017.11:33238757:G:A (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 rs9972931

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