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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.

rs13175786

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr5:7447412 (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>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.169020 (44738/264690, TOPMED)
C=0.103322 (21175/204942, ALFA)
C=0.164684 (23063/140044, GnomAD) (+ 19 more)
C=0.00704 (199/28258, 14KJPN)
C=0.00680 (114/16760, 8.3KJPN)
C=0.1666 (1067/6404, 1000G_30x)
C=0.1611 (807/5008, 1000G)
C=0.0763 (342/4480, Estonian)
C=0.0755 (291/3854, ALSPAC)
C=0.0868 (322/3708, TWINSUK)
C=0.0031 (9/2922, KOREAN)
C=0.1353 (282/2084, HGDP_Stanford)
C=0.0033 (6/1832, Korea1K)
C=0.2085 (342/1640, HapMap)
C=0.1664 (188/1130, Daghestan)
C=0.077 (77/998, GoNL)
C=0.070 (42/600, NorthernSweden)
C=0.222 (48/216, Qatari)
C=0.009 (2/216, Vietnamese)
T=0.381 (45/118, SGDP_PRJ)
C=0.15 (8/54, Ancient Sardinia)
C=0.07 (3/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ADCY2 : 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 204942 T=0.896678 C=0.103322
European Sub 174960 T=0.911688 C=0.088312
African Sub 9732 T=0.6523 C=0.3477
African Others Sub 348 T=0.606 C=0.394
African American Sub 9384 T=0.6540 C=0.3460
Asian Sub 704 T=0.987 C=0.013
East Asian Sub 558 T=0.991 C=0.009
Other Asian Sub 146 T=0.973 C=0.027
Latin American 1 Sub 844 T=0.800 C=0.200
Latin American 2 Sub 6910 T=0.9381 C=0.0619
South Asian Sub 5042 T=0.8070 C=0.1930
Other Sub 6750 T=0.8873 C=0.1127


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=0.830980 C=0.169020
Allele Frequency Aggregator Total Global 204942 T=0.896678 C=0.103322
Allele Frequency Aggregator European Sub 174960 T=0.911688 C=0.088312
Allele Frequency Aggregator African Sub 9732 T=0.6523 C=0.3477
Allele Frequency Aggregator Latin American 2 Sub 6910 T=0.9381 C=0.0619
Allele Frequency Aggregator Other Sub 6750 T=0.8873 C=0.1127
Allele Frequency Aggregator South Asian Sub 5042 T=0.8070 C=0.1930
Allele Frequency Aggregator Latin American 1 Sub 844 T=0.800 C=0.200
Allele Frequency Aggregator Asian Sub 704 T=0.987 C=0.013
gnomAD - Genomes Global Study-wide 140044 T=0.835316 C=0.164684
gnomAD - Genomes European Sub 75900 T=0.91368 C=0.08632
gnomAD - Genomes African Sub 41894 T=0.65138 C=0.34862
gnomAD - Genomes American Sub 13652 T=0.90551 C=0.09449
gnomAD - Genomes Ashkenazi Jewish Sub 3324 T=0.9085 C=0.0915
gnomAD - Genomes East Asian Sub 3126 T=0.9930 C=0.0070
gnomAD - Genomes Other Sub 2148 T=0.8650 C=0.1350
14KJPN JAPANESE Study-wide 28258 T=0.99296 C=0.00704
8.3KJPN JAPANESE Study-wide 16760 T=0.99320 C=0.00680
1000Genomes_30x Global Study-wide 6404 T=0.8334 C=0.1666
1000Genomes_30x African Sub 1786 T=0.6153 C=0.3847
1000Genomes_30x Europe Sub 1266 T=0.9226 C=0.0774
1000Genomes_30x South Asian Sub 1202 T=0.8295 C=0.1705
1000Genomes_30x East Asian Sub 1170 T=0.9949 C=0.0051
1000Genomes_30x American Sub 980 T=0.928 C=0.072
1000Genomes Global Study-wide 5008 T=0.8389 C=0.1611
1000Genomes African Sub 1322 T=0.6256 C=0.3744
1000Genomes East Asian Sub 1008 T=0.9940 C=0.0060
1000Genomes Europe Sub 1006 T=0.9225 C=0.0775
1000Genomes South Asian Sub 978 T=0.819 C=0.181
1000Genomes American Sub 694 T=0.927 C=0.073
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.9237 C=0.0763
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.9245 C=0.0755
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.9132 C=0.0868
KOREAN population from KRGDB KOREAN Study-wide 2922 T=0.9969 C=0.0031
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 T=0.8647 C=0.1353
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 T=0.979 C=0.021
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 T=0.797 C=0.203
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 T=0.840 C=0.160
HGDP-CEPH-db Supplement 1 Europe Sub 320 T=0.925 C=0.075
HGDP-CEPH-db Supplement 1 Africa Sub 242 T=0.570 C=0.430
HGDP-CEPH-db Supplement 1 America Sub 216 T=0.995 C=0.005
HGDP-CEPH-db Supplement 1 Oceania Sub 72 T=0.96 C=0.04
Korean Genome Project KOREAN Study-wide 1832 T=0.9967 C=0.0033
HapMap Global Study-wide 1640 T=0.7915 C=0.2085
HapMap African Sub 692 T=0.649 C=0.351
HapMap American Sub 600 T=0.865 C=0.135
HapMap Europe Sub 176 T=0.915 C=0.085
HapMap Asian Sub 172 T=0.983 C=0.017
Genome-wide autozygosity in Daghestan Global Study-wide 1130 T=0.8336 C=0.1664
Genome-wide autozygosity in Daghestan Daghestan Sub 628 T=0.822 C=0.178
Genome-wide autozygosity in Daghestan Near_East Sub 142 T=0.789 C=0.211
Genome-wide autozygosity in Daghestan Central Asia Sub 118 T=0.941 C=0.059
Genome-wide autozygosity in Daghestan Europe Sub 108 T=0.926 C=0.074
Genome-wide autozygosity in Daghestan South Asian Sub 98 T=0.80 C=0.20
Genome-wide autozygosity in Daghestan Caucasus Sub 36 T=0.69 C=0.31
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.923 C=0.077
Northern Sweden ACPOP Study-wide 600 T=0.930 C=0.070
Qatari Global Study-wide 216 T=0.778 C=0.222
A Vietnamese Genetic Variation Database Global Study-wide 216 T=0.991 C=0.009
SGDP_PRJ Global Study-wide 118 T=0.381 C=0.619
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 54 T=0.85 C=0.15
The Danish reference pan genome Danish Study-wide 40 T=0.93 C=0.07
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 5 NC_000005.10:g.7447412T>C
GRCh37.p13 chr 5 NC_000005.9:g.7447525T>C
ADCY2 RefSeqGene NG_046913.1:g.56183T>C
Gene: ADCY2, adenylate cyclase 2 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
ADCY2 transcript NM_020546.3:c.408+32642T>C N/A Intron Variant
ADCY2 transcript variant X2 XM_011513942.3:c.408+3264…

XM_011513942.3:c.408+32642T>C

N/A Intron Variant
ADCY2 transcript variant X1 XM_047416645.1:c.408+3264…

XM_047416645.1:c.408+32642T>C

N/A Intron Variant
ADCY2 transcript variant X3 XM_047416646.1:c.408+3264…

XM_047416646.1:c.408+32642T>C

N/A Intron Variant
ADCY2 transcript variant X4 XM_047416647.1:c.408+3264…

XM_047416647.1:c.408+32642T>C

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 T= C
GRCh38.p14 chr 5 NC_000005.10:g.7447412= NC_000005.10:g.7447412T>C
GRCh37.p13 chr 5 NC_000005.9:g.7447525= NC_000005.9:g.7447525T>C
ADCY2 RefSeqGene NG_046913.1:g.56183= NG_046913.1:g.56183T>C
ADCY2 transcript NM_020546.2:c.408+32642= NM_020546.2:c.408+32642T>C
ADCY2 transcript NM_020546.3:c.408+32642= NM_020546.3:c.408+32642T>C
ADCY2 transcript variant X2 XM_011513942.3:c.408+32642= XM_011513942.3:c.408+32642T>C
ADCY2 transcript variant X1 XM_047416645.1:c.408+32642= XM_047416645.1:c.408+32642T>C
ADCY2 transcript variant X3 XM_047416646.1:c.408+32642= XM_047416646.1:c.408+32642T>C
ADCY2 transcript variant X4 XM_047416647.1:c.408+32642= XM_047416647.1:c.408+32642T>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#.

103 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 SSAHASNP ss22309279 Apr 05, 2004 (121)
2 ABI ss44586274 Mar 15, 2006 (126)
3 ILLUMINA ss66799393 Dec 02, 2006 (127)
4 ILLUMINA ss67062197 Dec 02, 2006 (127)
5 ILLUMINA ss67390153 Dec 02, 2006 (127)
6 ILLUMINA ss70420173 May 18, 2007 (127)
7 ILLUMINA ss70596603 May 25, 2008 (130)
8 ILLUMINA ss71141118 May 18, 2007 (127)
9 ILLUMINA ss75814171 Dec 07, 2007 (129)
10 KRIBB_YJKIM ss85306101 Dec 15, 2007 (130)
11 1000GENOMES ss111381583 Jan 25, 2009 (130)
12 ILLUMINA ss121624704 Dec 01, 2009 (131)
13 ILLUMINA ss153328755 Dec 01, 2009 (131)
14 ILLUMINA ss159247636 Dec 01, 2009 (131)
15 ILLUMINA ss160321325 Dec 01, 2009 (131)
16 COMPLETE_GENOMICS ss164160339 Jul 04, 2010 (132)
17 ILLUMINA ss170307524 Jul 04, 2010 (132)
18 ILLUMINA ss172345694 Jul 04, 2010 (132)
19 BUSHMAN ss199845151 Jul 04, 2010 (132)
20 1000GENOMES ss221500720 Jul 14, 2010 (132)
21 1000GENOMES ss232816994 Jul 14, 2010 (132)
22 1000GENOMES ss240016761 Jul 15, 2010 (132)
23 ILLUMINA ss479882685 May 04, 2012 (137)
24 ILLUMINA ss479890570 May 04, 2012 (137)
25 ILLUMINA ss480502011 Sep 08, 2015 (146)
26 ILLUMINA ss484739826 May 04, 2012 (137)
27 ILLUMINA ss536836535 Sep 08, 2015 (146)
28 TISHKOFF ss558185315 Apr 25, 2013 (138)
29 SSMP ss652030272 Apr 25, 2013 (138)
30 ILLUMINA ss778422378 Aug 21, 2014 (142)
31 ILLUMINA ss782816600 Aug 21, 2014 (142)
32 ILLUMINA ss783781752 Aug 21, 2014 (142)
33 ILLUMINA ss825389447 Apr 01, 2015 (144)
34 ILLUMINA ss832069888 Apr 01, 2015 (144)
35 ILLUMINA ss832759917 Aug 21, 2014 (142)
36 ILLUMINA ss833350747 Aug 21, 2014 (142)
37 ILLUMINA ss833877753 Aug 21, 2014 (142)
38 EVA-GONL ss981220970 Aug 21, 2014 (142)
39 JMKIDD_LAB ss1072368562 Aug 21, 2014 (142)
40 1000GENOMES ss1313804907 Aug 21, 2014 (142)
41 HAMMER_LAB ss1397404177 Sep 08, 2015 (146)
42 EVA_GENOME_DK ss1580999867 Apr 01, 2015 (144)
43 EVA_DECODE ss1590736497 Apr 01, 2015 (144)
44 EVA_UK10K_ALSPAC ss1612220799 Apr 01, 2015 (144)
45 EVA_UK10K_TWINSUK ss1655214832 Apr 01, 2015 (144)
46 EVA_SVP ss1712741740 Apr 01, 2015 (144)
47 ILLUMINA ss1752584190 Sep 08, 2015 (146)
48 HAMMER_LAB ss1803018471 Sep 08, 2015 (146)
49 WEILL_CORNELL_DGM ss1924480044 Feb 12, 2016 (147)
50 GENOMED ss1970005853 Jul 19, 2016 (147)
51 JJLAB ss2022835713 Sep 14, 2016 (149)
52 ILLUMINA ss2095153173 Dec 20, 2016 (150)
53 HUMAN_LONGEVITY ss2271169156 Dec 20, 2016 (150)
54 ILLUMINA ss2634242390 Nov 08, 2017 (151)
55 GNOMAD ss2820874165 Nov 08, 2017 (151)
56 AFFY ss2985943534 Nov 08, 2017 (151)
57 SWEGEN ss2996397975 Nov 08, 2017 (151)
58 BIOINF_KMB_FNS_UNIBA ss3025202297 Nov 08, 2017 (151)
59 CSHL ss3346229860 Nov 08, 2017 (151)
60 ILLUMINA ss3629172017 Oct 12, 2018 (152)
61 ILLUMINA ss3632171348 Oct 12, 2018 (152)
62 ILLUMINA ss3633364552 Oct 12, 2018 (152)
63 ILLUMINA ss3634084755 Oct 12, 2018 (152)
64 ILLUMINA ss3634990010 Oct 12, 2018 (152)
65 ILLUMINA ss3635767003 Oct 12, 2018 (152)
66 ILLUMINA ss3636699228 Oct 12, 2018 (152)
67 ILLUMINA ss3637519607 Oct 12, 2018 (152)
68 ILLUMINA ss3638536940 Oct 12, 2018 (152)
69 ILLUMINA ss3639271084 Oct 12, 2018 (152)
70 ILLUMINA ss3639658341 Oct 12, 2018 (152)
71 ILLUMINA ss3640697303 Oct 12, 2018 (152)
72 ILLUMINA ss3643484155 Oct 12, 2018 (152)
73 URBANLAB ss3647979433 Oct 12, 2018 (152)
74 ILLUMINA ss3652956641 Oct 12, 2018 (152)
75 EGCUT_WGS ss3664287019 Jul 13, 2019 (153)
76 EVA_DECODE ss3714055530 Jul 13, 2019 (153)
77 ACPOP ss3732065875 Jul 13, 2019 (153)
78 ILLUMINA ss3745290154 Jul 13, 2019 (153)
79 EVA ss3763034921 Jul 13, 2019 (153)
80 ILLUMINA ss3772784526 Jul 13, 2019 (153)
81 KHV_HUMAN_GENOMES ss3806201717 Jul 13, 2019 (153)
82 EVA ss3829081065 Apr 26, 2020 (154)
83 HGDP ss3847780529 Apr 26, 2020 (154)
84 SGDP_PRJ ss3861158821 Apr 26, 2020 (154)
85 KRGDB ss3907600573 Apr 26, 2020 (154)
86 KOGIC ss3956050189 Apr 26, 2020 (154)
87 EVA ss3985123428 Apr 26, 2021 (155)
88 EVA ss4017191674 Apr 26, 2021 (155)
89 TOPMED ss4648762991 Apr 26, 2021 (155)
90 TOMMO_GENOMICS ss5170271440 Apr 26, 2021 (155)
91 1000G_HIGH_COVERAGE ss5262789769 Oct 13, 2022 (156)
92 EVA ss5315030138 Oct 13, 2022 (156)
93 EVA ss5355492957 Oct 13, 2022 (156)
94 HUGCELL_USP ss5461143593 Oct 13, 2022 (156)
95 1000G_HIGH_COVERAGE ss5545794092 Oct 13, 2022 (156)
96 SANFORD_IMAGENETICS ss5637133111 Oct 13, 2022 (156)
97 TOMMO_GENOMICS ss5705914886 Oct 13, 2022 (156)
98 EVA ss5799640511 Oct 13, 2022 (156)
99 YY_MCH ss5805999067 Oct 13, 2022 (156)
100 EVA ss5834484324 Oct 13, 2022 (156)
101 EVA ss5854670553 Oct 13, 2022 (156)
102 EVA ss5892890393 Oct 13, 2022 (156)
103 EVA ss5965542334 Oct 13, 2022 (156)
104 1000Genomes NC_000005.9 - 7447525 Oct 12, 2018 (152)
105 1000Genomes_30x NC_000005.10 - 7447412 Oct 13, 2022 (156)
106 The Avon Longitudinal Study of Parents and Children NC_000005.9 - 7447525 Oct 12, 2018 (152)
107 Genome-wide autozygosity in Daghestan NC_000005.8 - 7500525 Apr 26, 2020 (154)
108 Genetic variation in the Estonian population NC_000005.9 - 7447525 Oct 12, 2018 (152)
109 The Danish reference pan genome NC_000005.9 - 7447525 Apr 26, 2020 (154)
110 gnomAD - Genomes NC_000005.10 - 7447412 Apr 26, 2021 (155)
111 Genome of the Netherlands Release 5 NC_000005.9 - 7447525 Apr 26, 2020 (154)
112 HGDP-CEPH-db Supplement 1 NC_000005.8 - 7500525 Apr 26, 2020 (154)
113 HapMap NC_000005.10 - 7447412 Apr 26, 2020 (154)
114 KOREAN population from KRGDB NC_000005.9 - 7447525 Apr 26, 2020 (154)
115 Korean Genome Project NC_000005.10 - 7447412 Apr 26, 2020 (154)
116 Northern Sweden NC_000005.9 - 7447525 Jul 13, 2019 (153)
117 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000005.9 - 7447525 Apr 26, 2021 (155)
118 Qatari NC_000005.9 - 7447525 Apr 26, 2020 (154)
119 SGDP_PRJ NC_000005.9 - 7447525 Apr 26, 2020 (154)
120 8.3KJPN NC_000005.9 - 7447525 Apr 26, 2021 (155)
121 14KJPN NC_000005.10 - 7447412 Oct 13, 2022 (156)
122 TopMed NC_000005.10 - 7447412 Apr 26, 2021 (155)
123 UK 10K study - Twins NC_000005.9 - 7447525 Oct 12, 2018 (152)
124 A Vietnamese Genetic Variation Database NC_000005.9 - 7447525 Jul 13, 2019 (153)
125 ALFA NC_000005.10 - 7447412 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)
rs59464947 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
379327, 458421, ss111381583, ss160321325, ss164160339, ss199845151, ss479882685, ss825389447, ss1397404177, ss1590736497, ss1712741740, ss3639271084, ss3639658341, ss3643484155, ss3847780529 NC_000005.8:7500524:T:C NC_000005.10:7447411:T:C (self)
25356063, 14106299, 10025267, 7164806, 6262790, 14777967, 5350740, 349355, 6521974, 13175801, 28240747, 14106299, 3128867, ss221500720, ss232816994, ss240016761, ss479890570, ss480502011, ss484739826, ss536836535, ss558185315, ss652030272, ss778422378, ss782816600, ss783781752, ss832069888, ss832759917, ss833350747, ss833877753, ss981220970, ss1072368562, ss1313804907, ss1580999867, ss1612220799, ss1655214832, ss1752584190, ss1803018471, ss1924480044, ss1970005853, ss2022835713, ss2095153173, ss2634242390, ss2820874165, ss2985943534, ss2996397975, ss3346229860, ss3629172017, ss3632171348, ss3633364552, ss3634084755, ss3634990010, ss3635767003, ss3636699228, ss3637519607, ss3638536940, ss3640697303, ss3652956641, ss3664287019, ss3732065875, ss3745290154, ss3763034921, ss3772784526, ss3829081065, ss3861158821, ss3907600573, ss3985123428, ss4017191674, ss5170271440, ss5315030138, ss5355492957, ss5637133111, ss5799640511, ss5834484324, ss5965542334 NC_000005.9:7447524:T:C NC_000005.10:7447411:T:C (self)
33320027, 179216319, 2802590, 12428190, 39751990, 486140548, 12957486743, ss2271169156, ss3025202297, ss3647979433, ss3714055530, ss3806201717, ss3956050189, ss4648762991, ss5262789769, ss5461143593, ss5545794092, ss5705914886, ss5805999067, ss5854670553, ss5892890393 NC_000005.10:7447411:T:C NC_000005.10:7447411:T:C (self)
ss44586274, ss66799393, ss67062197, ss67390153, ss70420173, ss70596603, ss71141118, ss75814171, ss85306101, ss121624704, ss153328755, ss159247636, ss170307524, ss172345694 NT_006576.16:7437524:T:C NC_000005.10:7447411:T:C (self)
ss22309279 NT_023089.13:7430262:T:C NC_000005.10:7447411:T:C (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 rs13175786

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