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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.

rs17290760

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr9:32556382 (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
A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.096849 (25635/264690, TOPMED)
G=0.140106 (24268/173212, ALFA)
G=0.103601 (14530/140250, GnomAD) (+ 21 more)
G=0.05581 (4392/78690, PAGE_STUDY)
G=0.00970 (274/28258, 14KJPN)
G=0.01062 (178/16760, 8.3KJPN)
G=0.0589 (377/6404, 1000G_30x)
G=0.0603 (302/5008, 1000G)
G=0.1386 (621/4480, Estonian)
G=0.1432 (552/3854, ALSPAC)
G=0.1262 (468/3708, TWINSUK)
G=0.0161 (47/2922, KOREAN)
G=0.0950 (198/2084, HGDP_Stanford)
G=0.0772 (137/1774, HapMap)
G=0.123 (123/998, GoNL)
G=0.027 (21/792, PRJEB37584)
G=0.157 (94/600, NorthernSweden)
G=0.199 (43/216, Qatari)
G=0.009 (2/212, Vietnamese)
G=0.28 (24/86, Ancient Sardinia)
A=0.47 (38/80, SGDP_PRJ)
G=0.10 (4/40, GENOME_DK)
A=0.5 (3/6, Siberian)
G=0.5 (3/6, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SMIM27 : Intron Variant
NDUFB6 : Intron Variant
Publications
1 citation
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 178246 A=0.860670 G=0.139330 0.742311 0.020971 0.236718 9
European Sub 156576 A=0.850954 G=0.149046 0.724492 0.022583 0.252925 0
African Sub 6530 A=0.9654 G=0.0346 0.931394 0.000613 0.067994 1
African Others Sub 278 A=0.986 G=0.014 0.971223 0.0 0.028777 0
African American Sub 6252 A=0.9645 G=0.0355 0.929623 0.00064 0.069738 1
Asian Sub 3428 A=0.9737 G=0.0263 0.948075 0.000583 0.051342 0
East Asian Sub 2786 A=0.9846 G=0.0154 0.969131 0.0 0.030869 0
Other Asian Sub 642 A=0.927 G=0.073 0.856698 0.003115 0.140187 0
Latin American 1 Sub 544 A=0.857 G=0.143 0.742647 0.029412 0.227941 1
Latin American 2 Sub 1550 A=0.9142 G=0.0858 0.837419 0.009032 0.153548 0
South Asian Sub 5134 A=0.9266 G=0.0734 0.861317 0.008181 0.130503 3
Other Sub 4484 A=0.8675 G=0.1325 0.762712 0.027654 0.209634 10


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=0.903151 G=0.096849
Allele Frequency Aggregator Total Global 173212 A=0.859894 G=0.140106
Allele Frequency Aggregator European Sub 153482 A=0.850986 G=0.149014
Allele Frequency Aggregator African Sub 5390 A=0.9649 G=0.0351
Allele Frequency Aggregator South Asian Sub 5134 A=0.9266 G=0.0734
Allele Frequency Aggregator Other Sub 3684 A=0.8561 G=0.1439
Allele Frequency Aggregator Asian Sub 3428 A=0.9737 G=0.0263
Allele Frequency Aggregator Latin American 2 Sub 1550 A=0.9142 G=0.0858
Allele Frequency Aggregator Latin American 1 Sub 544 A=0.857 G=0.143
gnomAD - Genomes Global Study-wide 140250 A=0.896399 G=0.103601
gnomAD - Genomes European Sub 75936 A=0.85511 G=0.14489
gnomAD - Genomes African Sub 42048 A=0.96742 G=0.03258
gnomAD - Genomes American Sub 13658 A=0.91068 G=0.08932
gnomAD - Genomes Ashkenazi Jewish Sub 3324 A=0.7963 G=0.2037
gnomAD - Genomes East Asian Sub 3134 A=0.9872 G=0.0128
gnomAD - Genomes Other Sub 2150 A=0.8972 G=0.1028
The PAGE Study Global Study-wide 78690 A=0.94419 G=0.05581
The PAGE Study AfricanAmerican Sub 32514 A=0.96565 G=0.03435
The PAGE Study Mexican Sub 10806 A=0.93772 G=0.06228
The PAGE Study Asian Sub 8312 A=0.9847 G=0.0153
The PAGE Study PuertoRican Sub 7918 A=0.8814 G=0.1186
The PAGE Study NativeHawaiian Sub 4534 A=0.9413 G=0.0587
The PAGE Study Cuban Sub 4230 A=0.8783 G=0.1217
The PAGE Study Dominican Sub 3828 A=0.9258 G=0.0742
The PAGE Study CentralAmerican Sub 2450 A=0.9412 G=0.0588
The PAGE Study SouthAmerican Sub 1982 A=0.9228 G=0.0772
The PAGE Study NativeAmerican Sub 1260 A=0.9040 G=0.0960
The PAGE Study SouthAsian Sub 856 A=0.938 G=0.062
14KJPN JAPANESE Study-wide 28258 A=0.99030 G=0.00970
8.3KJPN JAPANESE Study-wide 16760 A=0.98938 G=0.01062
1000Genomes_30x Global Study-wide 6404 A=0.9411 G=0.0589
1000Genomes_30x African Sub 1786 A=0.9888 G=0.0112
1000Genomes_30x Europe Sub 1266 A=0.8649 G=0.1351
1000Genomes_30x South Asian Sub 1202 A=0.9384 G=0.0616
1000Genomes_30x East Asian Sub 1170 A=0.9889 G=0.0111
1000Genomes_30x American Sub 980 A=0.899 G=0.101
1000Genomes Global Study-wide 5008 A=0.9397 G=0.0603
1000Genomes African Sub 1322 A=0.9864 G=0.0136
1000Genomes East Asian Sub 1008 A=0.9881 G=0.0119
1000Genomes Europe Sub 1006 A=0.8598 G=0.1402
1000Genomes South Asian Sub 978 A=0.934 G=0.066
1000Genomes American Sub 694 A=0.905 G=0.095
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.8614 G=0.1386
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.8568 G=0.1432
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.8738 G=0.1262
KOREAN population from KRGDB KOREAN Study-wide 2922 A=0.9839 G=0.0161
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 A=0.9050 G=0.0950
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.968 G=0.032
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.913 G=0.087
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.729 G=0.271
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.878 G=0.122
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.988 G=0.012
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.995 G=0.005
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.88 G=0.12
HapMap Global Study-wide 1774 A=0.9228 G=0.0772
HapMap American Sub 760 A=0.921 G=0.079
HapMap African Sub 584 A=0.942 G=0.058
HapMap Asian Sub 254 A=0.972 G=0.028
HapMap Europe Sub 176 A=0.795 G=0.205
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.877 G=0.123
CNV burdens in cranial meningiomas Global Study-wide 792 A=0.973 G=0.027
CNV burdens in cranial meningiomas CRM Sub 792 A=0.973 G=0.027
Northern Sweden ACPOP Study-wide 600 A=0.843 G=0.157
Qatari Global Study-wide 216 A=0.801 G=0.199
A Vietnamese Genetic Variation Database Global Study-wide 212 A=0.991 G=0.009
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 86 A=0.72 G=0.28
SGDP_PRJ Global Study-wide 80 A=0.47 G=0.53
The Danish reference pan genome Danish Study-wide 40 A=0.90 G=0.10
Siberian Global Study-wide 6 A=0.5 G=0.5
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 9 NC_000009.12:g.32556382A>G
GRCh37.p13 chr 9 NC_000009.11:g.32556380A>G
NDUFB6 RefSeqGene NG_011511.1:g.21803T>C
TOPORS RefSeqGene NG_017050.1:g.1243T>C
Gene: NDUFB6, NADH:ubiquinone oxidoreductase subunit B6 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
NDUFB6 transcript variant 3 NM_001199987.2:c.226-2438…

NM_001199987.2:c.226-2438T>C

 		N/A Intron Variant
NDUFB6 transcript variant 1 NM_002493.5:c.319-2438T>C N/A Intron Variant
NDUFB6 transcript variant 2 NM_182739.3:c.274-2438T>C N/A Intron Variant
Gene: SMIM27, small integral membrane protein 27 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
SMIM27 transcript variant 1 NM_001349118.1:c. N/A Genic Downstream Transcript Variant
SMIM27 transcript variant 2 NM_001349119.2:c. N/A Genic Downstream Transcript Variant
SMIM27 transcript variant 5 NM_001387564.1:c. N/A Genic Downstream Transcript Variant
SMIM27 transcript variant 3 NR_146061.1:n. N/A Intron Variant
SMIM27 transcript variant 4 NR_146063.1: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
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= G
GRCh38.p14 chr 9 NC_000009.12:g.32556382= NC_000009.12:g.32556382A>G
GRCh37.p13 chr 9 NC_000009.11:g.32556380= NC_000009.11:g.32556380A>G
NDUFB6 RefSeqGene NG_011511.1:g.21803= NG_011511.1:g.21803T>C
TOPORS RefSeqGene NG_017050.1:g.1243= NG_017050.1:g.1243T>C
NDUFB6 transcript variant 3 NM_001199987.1:c.226-2438= NM_001199987.1:c.226-2438T>C
NDUFB6 transcript variant 3 NM_001199987.2:c.226-2438= NM_001199987.2:c.226-2438T>C
NDUFB6 transcript variant 1 NM_002493.4:c.319-2438= NM_002493.4:c.319-2438T>C
NDUFB6 transcript variant 1 NM_002493.5:c.319-2438= NM_002493.5:c.319-2438T>C
NDUFB6 transcript variant 2 NM_182739.2:c.274-2438= NM_182739.2:c.274-2438T>C
NDUFB6 transcript variant 2 NM_182739.3:c.274-2438= NM_182739.3:c.274-2438T>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#.

94 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 PERLEGEN ss24523002 Sep 20, 2004 (123)
2 ABI ss43485542 Mar 13, 2006 (126)
3 ILLUMINA ss67183140 Nov 29, 2006 (127)
4 ILLUMINA ss67553754 Nov 29, 2006 (127)
5 ILLUMINA ss68178999 Dec 12, 2006 (127)
6 ILLUMINA ss70661190 May 25, 2008 (130)
7 ILLUMINA ss71222400 May 16, 2007 (127)
8 ILLUMINA ss75874820 Dec 06, 2007 (129)
9 KRIBB_YJKIM ss85379886 Dec 15, 2007 (130)
10 HUMANGENOME_JCVI ss97794277 Feb 06, 2009 (130)
11 1000GENOMES ss108740602 Jan 23, 2009 (130)
12 ENSEMBL ss143580164 Dec 01, 2009 (131)
13 ILLUMINA ss153661915 Dec 01, 2009 (131)
14 ILLUMINA ss159315169 Dec 01, 2009 (131)
15 COMPLETE_GENOMICS ss164058533 Jul 04, 2010 (132)
16 ILLUMINA ss172802968 Jul 04, 2010 (132)
17 1000GENOMES ss234798510 Jul 15, 2010 (132)
18 ILLUMINA ss536962652 Sep 08, 2015 (146)
19 TISHKOFF ss561356306 Apr 25, 2013 (138)
20 SSMP ss655797851 Apr 25, 2013 (138)
21 ILLUMINA ss832827215 Aug 21, 2014 (142)
22 ILLUMINA ss833418045 Aug 21, 2014 (142)
23 EVA-GONL ss986504790 Aug 21, 2014 (142)
24 JMKIDD_LAB ss1076266893 Aug 21, 2014 (142)
25 1000GENOMES ss1333639919 Aug 21, 2014 (142)
26 DDI ss1431810221 Apr 01, 2015 (144)
27 EVA_GENOME_DK ss1583066942 Apr 01, 2015 (144)
28 EVA_DECODE ss1596142711 Apr 01, 2015 (144)
29 EVA_UK10K_ALSPAC ss1622636613 Apr 01, 2015 (144)
30 EVA_UK10K_TWINSUK ss1665630646 Apr 01, 2015 (144)
31 EVA_SVP ss1713105264 Apr 01, 2015 (144)
32 WEILL_CORNELL_DGM ss1929791172 Feb 12, 2016 (147)
33 ILLUMINA ss1946256780 Feb 12, 2016 (147)
34 ILLUMINA ss1959178450 Feb 12, 2016 (147)
35 JJLAB ss2025609018 Sep 14, 2016 (149)
36 USC_VALOUEV ss2153834855 Dec 20, 2016 (150)
37 HUMAN_LONGEVITY ss2310917133 Dec 20, 2016 (150)
38 ILLUMINA ss2634860239 Nov 08, 2017 (151)
39 GRF ss2709644547 Nov 08, 2017 (151)
40 ILLUMINA ss2711161848 Nov 08, 2017 (151)
41 GNOMAD ss2877487401 Nov 08, 2017 (151)
42 SWEGEN ss3004673801 Nov 08, 2017 (151)
43 ILLUMINA ss3022923297 Nov 08, 2017 (151)
44 BIOINF_KMB_FNS_UNIBA ss3026594290 Nov 08, 2017 (151)
45 CSHL ss3348611057 Nov 08, 2017 (151)
46 ILLUMINA ss3625982399 Oct 12, 2018 (152)
47 ILLUMINA ss3630253508 Oct 12, 2018 (152)
48 ILLUMINA ss3638810200 Oct 12, 2018 (152)
49 ILLUMINA ss3639410154 Oct 12, 2018 (152)
50 ILLUMINA ss3639997030 Oct 12, 2018 (152)
51 ILLUMINA ss3643737210 Oct 12, 2018 (152)
52 ILLUMINA ss3644039961 Oct 12, 2018 (152)
53 ILLUMINA ss3644990108 Oct 12, 2018 (152)
54 URBANLAB ss3649113484 Oct 12, 2018 (152)
55 ILLUMINA ss3653474843 Oct 12, 2018 (152)
56 EGCUT_WGS ss3672428476 Jul 13, 2019 (153)
57 EVA_DECODE ss3723825934 Jul 13, 2019 (153)
58 ILLUMINA ss3726607214 Jul 13, 2019 (153)
59 ACPOP ss3736470293 Jul 13, 2019 (153)
60 ILLUMINA ss3744318750 Jul 13, 2019 (153)
61 EVA ss3769141073 Jul 13, 2019 (153)
62 PAGE_CC ss3771496789 Jul 13, 2019 (153)
63 PACBIO ss3786395834 Jul 13, 2019 (153)
64 PACBIO ss3791615683 Jul 13, 2019 (153)
65 PACBIO ss3796497372 Jul 13, 2019 (153)
66 KHV_HUMAN_GENOMES ss3812299941 Jul 13, 2019 (153)
67 EVA ss3831631905 Apr 26, 2020 (154)
68 EVA ss3839333588 Apr 26, 2020 (154)
69 EVA ss3844796709 Apr 26, 2020 (154)
70 HGDP ss3847946913 Apr 26, 2020 (154)
71 SGDP_PRJ ss3871910485 Apr 26, 2020 (154)
72 KRGDB ss3919579424 Apr 26, 2020 (154)
73 EVA ss3984618953 Apr 26, 2021 (155)
74 EVA ss3985416831 Apr 26, 2021 (155)
75 EVA ss4017435534 Apr 26, 2021 (155)
76 TOPMED ss4819109637 Apr 26, 2021 (155)
77 TOMMO_GENOMICS ss5192890746 Apr 26, 2021 (155)
78 EVA ss5237458381 Apr 26, 2021 (155)
79 1000G_HIGH_COVERAGE ss5280429514 Oct 13, 2022 (156)
80 EVA ss5387195045 Oct 13, 2022 (156)
81 HUGCELL_USP ss5476642938 Oct 13, 2022 (156)
82 EVA ss5509697063 Oct 13, 2022 (156)
83 1000G_HIGH_COVERAGE ss5572546314 Oct 13, 2022 (156)
84 SANFORD_IMAGENETICS ss5624718245 Oct 13, 2022 (156)
85 SANFORD_IMAGENETICS ss5647279023 Oct 13, 2022 (156)
86 TOMMO_GENOMICS ss5736164419 Oct 13, 2022 (156)
87 YY_MCH ss5810503820 Oct 13, 2022 (156)
88 EVA ss5829095598 Oct 13, 2022 (156)
89 EVA ss5847355231 Oct 13, 2022 (156)
90 EVA ss5848203855 Oct 13, 2022 (156)
91 EVA ss5856750528 Oct 13, 2022 (156)
92 EVA ss5916254455 Oct 13, 2022 (156)
93 EVA ss5976560170 Oct 13, 2022 (156)
94 EVA ss5979891444 Oct 13, 2022 (156)
95 1000Genomes NC_000009.11 - 32556380 Oct 12, 2018 (152)
96 1000Genomes_30x NC_000009.12 - 32556382 Oct 13, 2022 (156)
97 The Avon Longitudinal Study of Parents and Children NC_000009.11 - 32556380 Oct 12, 2018 (152)
98 Genetic variation in the Estonian population NC_000009.11 - 32556380 Oct 12, 2018 (152)
99 The Danish reference pan genome NC_000009.11 - 32556380 Apr 26, 2020 (154)
100 gnomAD - Genomes NC_000009.12 - 32556382 Apr 26, 2021 (155)
101 Genome of the Netherlands Release 5 NC_000009.11 - 32556380 Apr 26, 2020 (154)
102 HGDP-CEPH-db Supplement 1 NC_000009.10 - 32546380 Apr 26, 2020 (154)
103 HapMap NC_000009.12 - 32556382 Apr 26, 2020 (154)
104 KOREAN population from KRGDB NC_000009.11 - 32556380 Apr 26, 2020 (154)
105 Northern Sweden NC_000009.11 - 32556380 Jul 13, 2019 (153)
106 The PAGE Study NC_000009.12 - 32556382 Jul 13, 2019 (153)
107 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000009.11 - 32556380 Apr 26, 2021 (155)
108 CNV burdens in cranial meningiomas NC_000009.11 - 32556380 Apr 26, 2021 (155)
109 Qatari NC_000009.11 - 32556380 Apr 26, 2020 (154)
110 SGDP_PRJ NC_000009.11 - 32556380 Apr 26, 2020 (154)
111 Siberian NC_000009.11 - 32556380 Apr 26, 2020 (154)
112 8.3KJPN NC_000009.11 - 32556380 Apr 26, 2021 (155)
113 14KJPN NC_000009.12 - 32556382 Oct 13, 2022 (156)
114 TopMed NC_000009.12 - 32556382 Apr 26, 2021 (155)
115 UK 10K study - Twins NC_000009.11 - 32556380 Oct 12, 2018 (152)
116 A Vietnamese Genetic Variation Database NC_000009.11 - 32556380 Jul 13, 2019 (153)
117 ALFA NC_000009.12 - 32556382 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)
rs60056153 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss3639410154, ss3639997030, ss3644039961 NC_000009.9:32546379:A:G NC_000009.12:32556381:A:G (self)
624805, ss108740602, ss164058533, ss1596142711, ss1713105264, ss3643737210, ss3847946913 NC_000009.10:32546379:A:G NC_000009.12:32556381:A:G (self)
45890852, 25526245, 18166724, 9231879, 11388217, 26756818, 9755158, 642758, 168399, 11833102, 23927465, 6351209, 50860053, 25526245, 5674944, ss234798510, ss536962652, ss561356306, ss655797851, ss832827215, ss833418045, ss986504790, ss1076266893, ss1333639919, ss1431810221, ss1583066942, ss1622636613, ss1665630646, ss1929791172, ss1946256780, ss1959178450, ss2025609018, ss2153834855, ss2634860239, ss2709644547, ss2711161848, ss2877487401, ss3004673801, ss3022923297, ss3348611057, ss3625982399, ss3630253508, ss3638810200, ss3644990108, ss3653474843, ss3672428476, ss3736470293, ss3744318750, ss3769141073, ss3786395834, ss3791615683, ss3796497372, ss3831631905, ss3839333588, ss3871910485, ss3919579424, ss3984618953, ss3985416831, ss4017435534, ss5192890746, ss5237458381, ss5387195045, ss5509697063, ss5624718245, ss5647279023, ss5829095598, ss5847355231, ss5848203855, ss5976560170, ss5979891444 NC_000009.11:32556379:A:G NC_000009.12:32556381:A:G (self)
60072249, 323403208, 3821397, 718258, 70001523, 656487198, 5007557234, ss2310917133, ss3026594290, ss3649113484, ss3723825934, ss3726607214, ss3771496789, ss3812299941, ss3844796709, ss4819109637, ss5280429514, ss5476642938, ss5572546314, ss5736164419, ss5810503820, ss5856750528, ss5916254455 NC_000009.12:32556381:A:G NC_000009.12:32556381:A:G (self)
ss24523002, ss43485542, ss67183140, ss67553754, ss68178999, ss70661190, ss71222400, ss75874820, ss85379886, ss97794277, ss143580164, ss153661915, ss159315169, ss172802968 NT_008413.18:32546379:A:G NC_000009.12:32556381:A:G (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

1 citation for rs17290760
PMID Title Author Year Journal
22610502 Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. Kennedy RB et al. 2012 Human genetics
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