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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.

rs622450

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:20092847 (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 / G>C / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.090045 (23834/264690, TOPMED)
G=0.097730 (13707/140254, GnomAD)
G=0.13025 (8862/68036, ALFA) (+ 19 more)
G=0.00000 (0/28258, 14KJPN)
G=0.00000 (0/16760, 8.3KJPN)
G=0.0547 (350/6404, 1000G_30x)
G=0.0535 (268/5008, 1000G)
G=0.1431 (641/4480, Estonian)
G=0.1585 (611/3854, ALSPAC)
G=0.1478 (548/3708, TWINSUK)
G=0.0010 (3/2930, KOREAN)
G=0.0480 (100/2084, HGDP_Stanford)
G=0.0000 (0/1832, Korea1K)
G=0.0653 (94/1440, HapMap)
G=0.148 (148/998, GoNL)
G=0.202 (121/600, NorthernSweden)
G=0.031 (17/556, SGDP_PRJ)
G=0.028 (6/216, Qatari)
G=0.000 (0/212, Vietnamese)
G=0.09 (6/70, Ancient Sardinia)
G=0.09 (5/56, Siberian)
G=0.07 (3/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
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 68036 G=0.13025 A=0.00000, T=0.86975 0.01949 0.758981 0.22153 10
European Sub 55972 G=0.14588 A=0.00000, T=0.85412 0.022654 0.730901 0.246445 2
African Sub 4004 G=0.0282 A=0.0000, T=0.9718 0.001499 0.945055 0.053447 1
African Others Sub 146 G=0.000 A=0.000, T=1.000 0.0 1.0 0.0 N/A
African American Sub 3858 G=0.0293 A=0.0000, T=0.9707 0.001555 0.942976 0.055469 1
Asian Sub 190 G=0.005 A=0.000, T=0.995 0.0 0.989474 0.010526 0
East Asian Sub 148 G=0.000 A=0.000, T=1.000 0.0 1.0 0.0 N/A
Other Asian Sub 42 G=0.02 A=0.00, T=0.98 0.0 0.952381 0.047619 0
Latin American 1 Sub 254 G=0.079 A=0.000, T=0.921 0.0 0.84252 0.15748 1
Latin American 2 Sub 1232 G=0.0787 A=0.0000, T=0.9213 0.008117 0.850649 0.141234 0
South Asian Sub 4956 G=0.0686 A=0.0000, T=0.9314 0.004843 0.867635 0.127522 0
Other Sub 1428 G=0.0882 A=0.0000, T=0.9118 0.012605 0.836134 0.151261 2


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 G=0.090045 T=0.909955
gnomAD - Genomes Global Study-wide 140254 G=0.097730 T=0.902270
gnomAD - Genomes European Sub 75932 G=0.14330 T=0.85670
gnomAD - Genomes African Sub 42050 G=0.02606 T=0.97394
gnomAD - Genomes American Sub 13662 G=0.08579 T=0.91421
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=0.1086 T=0.8914
gnomAD - Genomes East Asian Sub 3134 G=0.0000 T=1.0000
gnomAD - Genomes Other Sub 2152 G=0.0915 T=0.9085
Allele Frequency Aggregator Total Global 68036 G=0.13025 A=0.00000, T=0.86975
Allele Frequency Aggregator European Sub 55972 G=0.14588 A=0.00000, T=0.85412
Allele Frequency Aggregator South Asian Sub 4956 G=0.0686 A=0.0000, T=0.9314
Allele Frequency Aggregator African Sub 4004 G=0.0282 A=0.0000, T=0.9718
Allele Frequency Aggregator Other Sub 1428 G=0.0882 A=0.0000, T=0.9118
Allele Frequency Aggregator Latin American 2 Sub 1232 G=0.0787 A=0.0000, T=0.9213
Allele Frequency Aggregator Latin American 1 Sub 254 G=0.079 A=0.000, T=0.921
Allele Frequency Aggregator Asian Sub 190 G=0.005 A=0.000, T=0.995
14KJPN JAPANESE Study-wide 28258 G=0.00000 T=1.00000
8.3KJPN JAPANESE Study-wide 16760 G=0.00000 T=1.00000
1000Genomes_30x Global Study-wide 6404 G=0.0547 T=0.9453
1000Genomes_30x African Sub 1786 G=0.0078 T=0.9922
1000Genomes_30x Europe Sub 1266 G=0.1572 T=0.8428
1000Genomes_30x South Asian Sub 1202 G=0.0458 T=0.9542
1000Genomes_30x East Asian Sub 1170 G=0.0000 T=1.0000
1000Genomes_30x American Sub 980 G=0.084 T=0.916
1000Genomes Global Study-wide 5008 G=0.0535 T=0.9465
1000Genomes African Sub 1322 G=0.0083 T=0.9917
1000Genomes East Asian Sub 1008 G=0.0000 T=1.0000
1000Genomes Europe Sub 1006 G=0.1561 T=0.8439
1000Genomes South Asian Sub 978 G=0.047 T=0.953
1000Genomes American Sub 694 G=0.078 T=0.922
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.1431 T=0.8569
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.1585 T=0.8415
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.1478 T=0.8522
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.0010 A=0.0000, C=0.0000, T=0.9990
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.0480 T=0.9520
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.004 T=0.996
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.085 T=0.915
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.040 T=0.960
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.144 T=0.856
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.000 T=1.000
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.014 T=0.986
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.00 T=1.00
Korean Genome Project KOREAN Study-wide 1832 G=0.0000 T=1.0000
HapMap Global Study-wide 1440 G=0.0653 T=0.9347
HapMap American Sub 770 G=0.087 T=0.913
HapMap African Sub 406 G=0.002 T=0.998
HapMap Europe Sub 176 G=0.148 T=0.852
HapMap Asian Sub 88 G=0.00 T=1.00
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.148 T=0.852
Northern Sweden ACPOP Study-wide 600 G=0.202 T=0.798
SGDP_PRJ Global Study-wide 556 G=0.031 T=0.969
Qatari Global Study-wide 216 G=0.028 T=0.972
A Vietnamese Genetic Variation Database Global Study-wide 212 G=0.000 T=1.000
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 70 G=0.09 T=0.91
Siberian Global Study-wide 56 G=0.09 T=0.91
The Danish reference pan genome Danish Study-wide 40 G=0.07 T=0.93
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.20092847G>A
GRCh38.p14 chr 1 NC_000001.11:g.20092847G>C
GRCh38.p14 chr 1 NC_000001.11:g.20092847G>T
GRCh37.p13 chr 1 NC_000001.10:g.20419340G>A
GRCh37.p13 chr 1 NC_000001.10:g.20419340G>C
GRCh37.p13 chr 1 NC_000001.10:g.20419340G>T
PLA2G5 RefSeqGene NG_032045.1:g.27640G>A
PLA2G5 RefSeqGene NG_032045.1:g.27640G>C
PLA2G5 RefSeqGene NG_032045.1:g.27640G>T
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 C T
GRCh38.p14 chr 1 NC_000001.11:g.20092847= NC_000001.11:g.20092847G>A NC_000001.11:g.20092847G>C NC_000001.11:g.20092847G>T
GRCh37.p13 chr 1 NC_000001.10:g.20419340= NC_000001.10:g.20419340G>A NC_000001.10:g.20419340G>C NC_000001.10:g.20419340G>T
PLA2G5 RefSeqGene NG_032045.1:g.27640= NG_032045.1:g.27640G>A NG_032045.1:g.27640G>C NG_032045.1:g.27640G>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#.

107 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss794869 Aug 11, 2000 (83)
2 KWOK ss1084812 Oct 04, 2000 (86)
3 KWOK ss1958131 Oct 18, 2000 (87)
4 TSC-CSHL ss2415782 Oct 23, 2000 (88)
5 SC_JCM ss2601574 Nov 09, 2000 (92)
6 SC_SNP ss13005205 Dec 05, 2003 (119)
7 EGP_SNPS ss16358139 Feb 27, 2004 (120)
8 CSHL-HAPMAP ss16426203 Feb 27, 2004 (120)
9 ABI ss44008513 Mar 14, 2006 (126)
10 ILLUMINA ss66590529 Dec 01, 2006 (127)
11 EGP_SNPS ss66858439 Dec 01, 2006 (127)
12 ILLUMINA ss67448259 Dec 01, 2006 (127)
13 ILLUMINA ss67799559 Dec 01, 2006 (127)
14 PERLEGEN ss68760640 May 18, 2007 (127)
15 ILLUMINA ss70861229 May 25, 2008 (130)
16 ILLUMINA ss71448542 May 18, 2007 (127)
17 ILLUMINA ss74946611 Dec 07, 2007 (129)
18 HGSV ss78250907 Dec 07, 2007 (129)
19 ILLUMINA ss79218360 Dec 15, 2007 (130)
20 HGSV ss81371174 Dec 15, 2007 (130)
21 KRIBB_YJKIM ss83500097 Dec 15, 2007 (130)
22 BCMHGSC_JDW ss87280431 Mar 23, 2008 (129)
23 BGI ss105128929 Dec 01, 2009 (131)
24 1000GENOMES ss108043929 Jan 22, 2009 (130)
25 1000GENOMES ss110150994 Jan 24, 2009 (130)
26 ILLUMINA-UK ss118546809 Feb 14, 2009 (130)
27 ILLUMINA ss122525662 Dec 01, 2009 (131)
28 ENSEMBL ss137832399 Dec 01, 2009 (131)
29 ILLUMINA ss154356226 Dec 01, 2009 (131)
30 GMI ss154732384 Dec 01, 2009 (131)
31 ILLUMINA ss159532493 Dec 01, 2009 (131)
32 COMPLETE_GENOMICS ss163152979 Jul 04, 2010 (132)
33 COMPLETE_GENOMICS ss163933691 Jul 04, 2010 (132)
34 COMPLETE_GENOMICS ss166201601 Jul 04, 2010 (132)
35 ILLUMINA ss172110287 Jul 04, 2010 (132)
36 ILLUMINA ss173990677 Jul 04, 2010 (132)
37 BUSHMAN ss198129501 Jul 04, 2010 (132)
38 BCM-HGSC-SUB ss205043774 Jul 04, 2010 (132)
39 1000GENOMES ss218271517 Jul 14, 2010 (132)
40 1000GENOMES ss230453144 Jul 14, 2010 (132)
41 ILLUMINA ss244304615 Jul 04, 2010 (132)
42 BL ss252965725 May 09, 2011 (134)
43 GMI ss275744109 May 04, 2012 (137)
44 GMI ss284014086 Apr 25, 2013 (138)
45 PJP ss290781319 May 09, 2011 (134)
46 ILLUMINA ss537343652 Sep 08, 2015 (146)
47 TISHKOFF ss553865539 Apr 25, 2013 (138)
48 SSMP ss647624599 Apr 25, 2013 (138)
49 ILLUMINA ss825548878 Apr 01, 2015 (144)
50 ILLUMINA ss833043733 Jul 12, 2019 (153)
51 EVA-GONL ss974922432 Aug 21, 2014 (142)
52 JMKIDD_LAB ss1067718206 Aug 21, 2014 (142)
53 1000GENOMES ss1289943697 Aug 21, 2014 (142)
54 DDI ss1425737563 Apr 01, 2015 (144)
55 EVA_GENOME_DK ss1573926409 Apr 01, 2015 (144)
56 EVA_DECODE ss1584280466 Apr 01, 2015 (144)
57 EVA_UK10K_ALSPAC ss1599678816 Apr 01, 2015 (144)
58 EVA_UK10K_TWINSUK ss1642672849 Apr 01, 2015 (144)
59 EVA_SVP ss1712316172 Apr 01, 2015 (144)
60 HAMMER_LAB ss1794022921 Sep 08, 2015 (146)
61 WEILL_CORNELL_DGM ss1918134262 Feb 12, 2016 (147)
62 GENOMED ss1966700019 Jul 19, 2016 (147)
63 JJLAB ss2019578767 Sep 14, 2016 (149)
64 USC_VALOUEV ss2147582215 Dec 20, 2016 (150)
65 HUMAN_LONGEVITY ss2160536254 Dec 20, 2016 (150)
66 SYSTEMSBIOZJU ss2624305685 Nov 08, 2017 (151)
67 GRF ss2697486773 Nov 08, 2017 (151)
68 GNOMAD ss2752400085 Nov 08, 2017 (151)
69 AFFY ss2985500911 Nov 08, 2017 (151)
70 SWEGEN ss2986427196 Nov 08, 2017 (151)
71 BIOINF_KMB_FNS_UNIBA ss3023554454 Nov 08, 2017 (151)
72 CSHL ss3343356007 Nov 08, 2017 (151)
73 ILLUMINA ss3626042607 Oct 11, 2018 (152)
74 ILLUMINA ss3637741471 Oct 11, 2018 (152)
75 ILLUMINA ss3638891743 Oct 11, 2018 (152)
76 ILLUMINA ss3639442893 Oct 11, 2018 (152)
77 ILLUMINA ss3642754950 Oct 11, 2018 (152)
78 EGCUT_WGS ss3654497466 Jul 12, 2019 (153)
79 EVA_DECODE ss3686297870 Jul 12, 2019 (153)
80 ACPOP ss3726849156 Jul 12, 2019 (153)
81 EVA ss3745912069 Jul 12, 2019 (153)
82 PACBIO ss3783346159 Jul 12, 2019 (153)
83 PACBIO ss3789016882 Jul 12, 2019 (153)
84 PACBIO ss3793889353 Jul 12, 2019 (153)
85 KHV_HUMAN_GENOMES ss3798932539 Jul 12, 2019 (153)
86 EVA ss3826058654 Apr 25, 2020 (154)
87 EVA ss3836417314 Apr 25, 2020 (154)
88 EVA ss3841821740 Apr 25, 2020 (154)
89 HGDP ss3847326592 Apr 25, 2020 (154)
90 SGDP_PRJ ss3848356934 Apr 25, 2020 (154)
91 KRGDB ss3893264915 Apr 25, 2020 (154)
92 KOGIC ss3943981473 Apr 25, 2020 (154)
93 EVA ss3984782734 Apr 26, 2021 (155)
94 TOPMED ss4441336014 Apr 26, 2021 (155)
95 TOMMO_GENOMICS ss5142817855 Apr 26, 2021 (155)
96 1000G_HIGH_COVERAGE ss5241425703 Oct 12, 2022 (156)
97 EVA ss5317185902 Oct 12, 2022 (156)
98 HUGCELL_USP ss5442584440 Oct 12, 2022 (156)
99 EVA ss5505782431 Oct 12, 2022 (156)
100 1000G_HIGH_COVERAGE ss5513294748 Oct 12, 2022 (156)
101 SANFORD_IMAGENETICS ss5625066803 Oct 12, 2022 (156)
102 TOMMO_GENOMICS ss5667220027 Oct 12, 2022 (156)
103 YY_MCH ss5800391637 Oct 12, 2022 (156)
104 EVA ss5831636076 Oct 12, 2022 (156)
105 EVA ss5848813405 Oct 12, 2022 (156)
106 EVA ss5907302535 Oct 12, 2022 (156)
107 EVA ss5936881920 Oct 12, 2022 (156)
108 1000Genomes NC_000001.10 - 20419340 Oct 11, 2018 (152)
109 1000Genomes_30x NC_000001.11 - 20092847 Oct 12, 2022 (156)
110 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 20419340 Oct 11, 2018 (152)
111 Genetic variation in the Estonian population NC_000001.10 - 20419340 Oct 11, 2018 (152)
112 The Danish reference pan genome NC_000001.10 - 20419340 Apr 25, 2020 (154)
113 gnomAD - Genomes NC_000001.11 - 20092847 Apr 26, 2021 (155)
114 Genome of the Netherlands Release 5 NC_000001.10 - 20419340 Apr 25, 2020 (154)
115 HGDP-CEPH-db Supplement 1 NC_000001.9 - 20291927 Apr 25, 2020 (154)
116 HapMap NC_000001.11 - 20092847 Apr 25, 2020 (154)
117 KOREAN population from KRGDB NC_000001.10 - 20419340 Apr 25, 2020 (154)
118 Korean Genome Project NC_000001.11 - 20092847 Apr 25, 2020 (154)
119 Northern Sweden NC_000001.10 - 20419340 Jul 12, 2019 (153)
120 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 20419340 Apr 26, 2021 (155)
121 Qatari NC_000001.10 - 20419340 Apr 25, 2020 (154)
122 SGDP_PRJ NC_000001.10 - 20419340 Apr 25, 2020 (154)
123 Siberian NC_000001.10 - 20419340 Apr 25, 2020 (154)
124 8.3KJPN NC_000001.10 - 20419340 Apr 26, 2021 (155)
125 14KJPN NC_000001.11 - 20092847 Oct 12, 2022 (156)
126 TopMed NC_000001.11 - 20092847 Apr 26, 2021 (155)
127 UK 10K study - Twins NC_000001.10 - 20419340 Oct 11, 2018 (152)
128 A Vietnamese Genetic Variation Database NC_000001.10 - 20419340 Jul 12, 2019 (153)
129 ALFA NC_000001.11 - 20092847 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)
rs1751970 Jan 18, 2001 (92)
rs60138044 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
442309, ss3893264915 NC_000001.10:20419339:G:A NC_000001.11:20092846:G:A (self)
3977173604 NC_000001.11:20092846:G:A NC_000001.11:20092846:G:A (self)
442309, ss3893264915 NC_000001.10:20419339:G:C NC_000001.11:20092846:G:C (self)
ss78250907, ss81371174, ss3638891743, ss3639442893 NC_000001.8:20164645:G:T NC_000001.11:20092846:G:T (self)
4484, ss87280431, ss108043929, ss110150994, ss118546809, ss163152979, ss163933691, ss166201601, ss198129501, ss205043774, ss252965725, ss275744109, ss284014086, ss290781319, ss825548878, ss1584280466, ss1712316172, ss3642754950, ss3847326592 NC_000001.9:20291926:G:T NC_000001.11:20092846:G:T (self)
628426, 330440, 235714, 1416547, 143721, 442309, 134021, 8661, 176192, 373914, 98569, 787162, 330440, 71032, ss218271517, ss230453144, ss537343652, ss553865539, ss647624599, ss833043733, ss974922432, ss1067718206, ss1289943697, ss1425737563, ss1573926409, ss1599678816, ss1642672849, ss1794022921, ss1918134262, ss1966700019, ss2019578767, ss2147582215, ss2624305685, ss2697486773, ss2752400085, ss2985500911, ss2986427196, ss3343356007, ss3626042607, ss3637741471, ss3654497466, ss3726849156, ss3745912069, ss3783346159, ss3789016882, ss3793889353, ss3826058654, ss3836417314, ss3848356934, ss3893264915, ss3984782734, ss5142817855, ss5317185902, ss5505782431, ss5625066803, ss5831636076, ss5936881920 NC_000001.10:20419339:G:T NC_000001.11:20092846:G:T (self)
820683, 4364416, 25742, 359474, 1057131, 4942349, 3977173604, ss2160536254, ss3023554454, ss3686297870, ss3798932539, ss3841821740, ss3943981473, ss4441336014, ss5241425703, ss5442584440, ss5513294748, ss5667220027, ss5800391637, ss5848813405, ss5907302535 NC_000001.11:20092846:G:T NC_000001.11:20092846:G:T (self)
ss13005205 NT_004610.15:1222589:G:T NC_000001.11:20092846:G:T (self)
ss16426203 NT_004610.16:1222589:G:T NC_000001.11:20092846:G:T (self)
ss794869, ss1084812, ss1958131, ss2415782, ss2601574, ss16358139, ss44008513, ss66590529, ss66858439, ss67448259, ss67799559, ss68760640, ss70861229, ss71448542, ss74946611, ss79218360, ss83500097, ss105128929, ss122525662, ss137832399, ss154356226, ss154732384, ss159532493, ss172110287, ss173990677, ss244304615 NT_004610.19:7099427:G:T NC_000001.11:20092846:G:T (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 rs622450
PMID Title Author Year Journal
19198613 Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. Gudmundsson J et al. 2009 Nature 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