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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.

rs821629

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:232011646 (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 / A>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.261831 (69304/264690, TOPMED)
T=0.278941 (39050/139994, GnomAD)
T=0.11346 (3206/28256, 14KJPN) (+ 17 more)
T=0.11038 (1850/16760, 8.3KJPN)
T=0.16843 (2327/13816, ALFA)
T=0.2453 (1571/6404, 1000G_30x)
T=0.2416 (1210/5008, 1000G)
T=0.2819 (1263/4480, Estonian)
T=0.2865 (1104/3854, ALSPAC)
T=0.2754 (1021/3708, TWINSUK)
T=0.1229 (360/2930, KOREAN)
T=0.1305 (239/1832, Korea1K)
T=0.282 (281/998, GoNL)
T=0.273 (164/600, NorthernSweden)
T=0.234 (72/308, HapMap)
A=0.376 (94/250, SGDP_PRJ)
T=0.245 (53/216, Qatari)
T=0.080 (17/212, Vietnamese)
T=0.30 (12/40, GENOME_DK)
A=0.41 (13/32, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
DISC1 : Intron Variant
TSNAX-DISC1 : 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 13816 A=0.83157 G=0.00000, T=0.16843
European Sub 10964 A=0.81056 G=0.00000, T=0.18944
African Sub 1688 A=0.8916 G=0.0000, T=0.1084
African Others Sub 68 A=0.90 G=0.00, T=0.10
African American Sub 1620 A=0.8914 G=0.0000, T=0.1086
Asian Sub 76 A=0.97 G=0.00, T=0.03
East Asian Sub 56 A=0.98 G=0.00, T=0.02
Other Asian Sub 20 A=0.95 G=0.00, T=0.05
Latin American 1 Sub 78 A=1.00 G=0.00, T=0.00
Latin American 2 Sub 460 A=1.000 G=0.000, T=0.000
South Asian Sub 58 A=1.00 G=0.00, T=0.00
Other Sub 492 A=0.868 G=0.000, T=0.132


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=0.738169 T=0.261831
gnomAD - Genomes Global Study-wide 139994 A=0.721059 T=0.278941
gnomAD - Genomes European Sub 75834 A=0.70700 T=0.29300
gnomAD - Genomes African Sub 41926 A=0.69728 T=0.30272
gnomAD - Genomes American Sub 13640 A=0.82214 T=0.17786
gnomAD - Genomes Ashkenazi Jewish Sub 3316 A=0.7603 T=0.2397
gnomAD - Genomes East Asian Sub 3130 A=0.8738 T=0.1262
gnomAD - Genomes Other Sub 2148 A=0.7565 T=0.2435
14KJPN JAPANESE Study-wide 28256 A=0.88654 T=0.11346
8.3KJPN JAPANESE Study-wide 16760 A=0.88962 T=0.11038
Allele Frequency Aggregator Total Global 13816 A=0.83157 G=0.00000, T=0.16843
Allele Frequency Aggregator European Sub 10964 A=0.81056 G=0.00000, T=0.18944
Allele Frequency Aggregator African Sub 1688 A=0.8916 G=0.0000, T=0.1084
Allele Frequency Aggregator Other Sub 492 A=0.868 G=0.000, T=0.132
Allele Frequency Aggregator Latin American 2 Sub 460 A=1.000 G=0.000, T=0.000
Allele Frequency Aggregator Latin American 1 Sub 78 A=1.00 G=0.00, T=0.00
Allele Frequency Aggregator Asian Sub 76 A=0.97 G=0.00, T=0.03
Allele Frequency Aggregator South Asian Sub 58 A=1.00 G=0.00, T=0.00
1000Genomes_30x Global Study-wide 6404 A=0.7547 T=0.2453
1000Genomes_30x African Sub 1786 A=0.6512 T=0.3488
1000Genomes_30x Europe Sub 1266 A=0.7172 T=0.2828
1000Genomes_30x South Asian Sub 1202 A=0.7304 T=0.2696
1000Genomes_30x East Asian Sub 1170 A=0.8915 T=0.1085
1000Genomes_30x American Sub 980 A=0.858 T=0.142
1000Genomes Global Study-wide 5008 A=0.7584 T=0.2416
1000Genomes African Sub 1322 A=0.6513 T=0.3487
1000Genomes East Asian Sub 1008 A=0.8909 T=0.1091
1000Genomes Europe Sub 1006 A=0.7177 T=0.2823
1000Genomes South Asian Sub 978 A=0.733 T=0.267
1000Genomes American Sub 694 A=0.865 T=0.135
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.7181 T=0.2819
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.7135 T=0.2865
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.7246 T=0.2754
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.8771 T=0.1229
Korean Genome Project KOREAN Study-wide 1832 A=0.8695 T=0.1305
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.718 T=0.282
Northern Sweden ACPOP Study-wide 600 A=0.727 T=0.273
HapMap Global Study-wide 308 A=0.766 T=0.234
HapMap African Sub 112 A=0.652 T=0.348
HapMap American Sub 108 A=0.741 T=0.259
HapMap Asian Sub 88 A=0.94 T=0.06
SGDP_PRJ Global Study-wide 250 A=0.376 T=0.624
Qatari Global Study-wide 216 A=0.755 T=0.245
A Vietnamese Genetic Variation Database Global Study-wide 212 A=0.920 T=0.080
The Danish reference pan genome Danish Study-wide 40 A=0.70 T=0.30
Siberian Global Study-wide 32 A=0.41 T=0.59
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.232011646A>G
GRCh38.p14 chr 1 NC_000001.11:g.232011646A>T
GRCh37.p13 chr 1 NC_000001.10:g.232147392A>G
GRCh37.p13 chr 1 NC_000001.10:g.232147392A>T
DISC1 RefSeqGene NG_011681.2:g.389832A>G
DISC1 RefSeqGene NG_011681.2:g.389832A>T
Gene: DISC1, DISC1 scaffold protein (plus strand)
Molecule type Change Amino acid[Codon] SO Term
DISC1 transcript variant Lv NM_001012957.2:c.2241+266…

NM_001012957.2:c.2241+2663A>G

 		N/A Intron Variant
DISC1 transcript variant a NM_001164537.2:c.2403+259…

NM_001164537.2:c.2403+2597A>G

 		N/A Intron Variant
DISC1 transcript variant d NM_001164540.2:c.1941+259…

NM_001164540.2:c.1941+2597A>G

 		N/A Intron Variant
DISC1 transcript variant L NM_018662.3:c.2307+2597A>G N/A Intron Variant
DISC1 transcript variant Es NM_001012958.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant S NM_001012959.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant b NM_001164538.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant c NM_001164539.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant e NM_001164541.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant f NM_001164542.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant g NM_001164544.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant h NM_001164545.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant i NM_001164546.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant j NM_001164547.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant k NM_001164548.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant l NM_001164549.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant m NM_001164550.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant n NM_001164551.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant o NM_001164552.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant p NM_001164553.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant q NM_001164554.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant r NM_001164555.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant t NM_001164556.2:c. N/A Genic Downstream Transcript Variant
Gene: TSNAX-DISC1, TSNAX-DISC1 readthrough (NMD candidate) (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TSNAX-DISC1 transcript variant 1 NR_028393.1:n. N/A Intron Variant
TSNAX-DISC1 transcript variant 2 NR_028394.1:n. N/A Genic Downstream Transcript Variant
TSNAX-DISC1 transcript variant 3 NR_028395.1:n. N/A Genic Downstream Transcript Variant
TSNAX-DISC1 transcript variant 4 NR_028396.1:n. N/A Genic Downstream Transcript Variant
TSNAX-DISC1 transcript variant 5 NR_028397.1:n. N/A Genic Downstream Transcript Variant
TSNAX-DISC1 transcript variant 6 NR_028398.1:n. N/A Genic Downstream Transcript Variant
TSNAX-DISC1 transcript variant 7 NR_028399.1:n. N/A Genic Downstream Transcript Variant
TSNAX-DISC1 transcript variant 8 NR_028400.1:n. N/A Genic Downstream Transcript 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 T
GRCh38.p14 chr 1 NC_000001.11:g.232011646= NC_000001.11:g.232011646A>G NC_000001.11:g.232011646A>T
GRCh37.p13 chr 1 NC_000001.10:g.232147392= NC_000001.10:g.232147392A>G NC_000001.10:g.232147392A>T
DISC1 RefSeqGene NG_011681.2:g.389832= NG_011681.2:g.389832A>G NG_011681.2:g.389832A>T
DISC1 transcript variant Lv NM_001012957.1:c.2241+2663= NM_001012957.1:c.2241+2663A>G NM_001012957.1:c.2241+2663A>T
DISC1 transcript variant Lv NM_001012957.2:c.2241+2663= NM_001012957.2:c.2241+2663A>G NM_001012957.2:c.2241+2663A>T
DISC1 transcript variant a NM_001164537.1:c.2403+2597= NM_001164537.1:c.2403+2597A>G NM_001164537.1:c.2403+2597A>T
DISC1 transcript variant a NM_001164537.2:c.2403+2597= NM_001164537.2:c.2403+2597A>G NM_001164537.2:c.2403+2597A>T
DISC1 transcript variant d NM_001164540.1:c.1941+2597= NM_001164540.1:c.1941+2597A>G NM_001164540.1:c.1941+2597A>T
DISC1 transcript variant d NM_001164540.2:c.1941+2597= NM_001164540.2:c.1941+2597A>G NM_001164540.2:c.1941+2597A>T
DISC1 transcript variant L NM_018662.2:c.2307+2597= NM_018662.2:c.2307+2597A>G NM_018662.2:c.2307+2597A>T
DISC1 transcript variant L NM_018662.3:c.2307+2597= NM_018662.3:c.2307+2597A>G NM_018662.3:c.2307+2597A>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#.

73 SubSNP, 20 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss1098614 Oct 05, 2000 (86)
2 KWOK ss1620240 Oct 18, 2000 (92)
3 SC_JCM ss2448891 Nov 08, 2000 (89)
4 SC_JCM ss3976226 Sep 28, 2001 (100)
5 CSHL-HAPMAP ss16433677 Feb 27, 2004 (120)
6 SSAHASNP ss20524003 Apr 05, 2004 (121)
7 ABI ss41084760 Mar 15, 2006 (126)
8 HGSV ss77456164 Dec 07, 2007 (129)
9 HGSV ss83487778 Dec 14, 2007 (130)
10 BCMHGSC_JDW ss88007038 Mar 23, 2008 (129)
11 HUMANGENOME_JCVI ss99295467 Feb 02, 2009 (130)
12 BGI ss106639030 Feb 02, 2009 (130)
13 1000GENOMES ss111928525 Jan 25, 2009 (130)
14 ILLUMINA-UK ss119244644 Feb 15, 2009 (130)
15 ENSEMBL ss138172328 Dec 01, 2009 (131)
16 ENSEMBL ss139038093 Dec 01, 2009 (131)
17 COMPLETE_GENOMICS ss165390378 Jul 04, 2010 (132)
18 COMPLETE_GENOMICS ss167561973 Jul 04, 2010 (132)
19 BUSHMAN ss199742133 Jul 04, 2010 (132)
20 BCM-HGSC-SUB ss205275892 Jul 04, 2010 (132)
21 1000GENOMES ss218938791 Jul 14, 2010 (132)
22 1000GENOMES ss230944650 Jul 14, 2010 (132)
23 1000GENOMES ss238550585 Jul 15, 2010 (132)
24 GMI ss276259652 May 04, 2012 (137)
25 GMI ss284246748 Apr 25, 2013 (138)
26 PJP ss290755147 May 09, 2011 (134)
27 TISHKOFF ss555206474 Apr 25, 2013 (138)
28 SSMP ss648779235 Apr 25, 2013 (138)
29 EVA-GONL ss976256226 Aug 21, 2014 (142)
30 JMKIDD_LAB ss1068685966 Aug 21, 2014 (142)
31 1000GENOMES ss1295071920 Aug 21, 2014 (142)
32 DDI ss1426143714 Apr 01, 2015 (144)
33 EVA_GENOME_DK ss1574749150 Apr 01, 2015 (144)
34 EVA_DECODE ss1585656031 Apr 01, 2015 (144)
35 EVA_UK10K_ALSPAC ss1602364501 Apr 01, 2015 (144)
36 EVA_UK10K_TWINSUK ss1645358534 Apr 01, 2015 (144)
37 HAMMER_LAB ss1795878848 Sep 08, 2015 (146)
38 WEILL_CORNELL_DGM ss1919477496 Feb 12, 2016 (147)
39 JJLAB ss2020263995 Sep 14, 2016 (149)
40 USC_VALOUEV ss2148300086 Dec 20, 2016 (150)
41 HUMAN_LONGEVITY ss2170956492 Dec 20, 2016 (150)
42 SYSTEMSBIOZJU ss2624644130 Nov 08, 2017 (151)
43 GRF ss2698300523 Nov 08, 2017 (151)
44 GNOMAD ss2767413330 Nov 08, 2017 (151)
45 SWEGEN ss2988623928 Nov 08, 2017 (151)
46 BIOINF_KMB_FNS_UNIBA ss3023892891 Nov 08, 2017 (151)
47 CSHL ss3343961201 Nov 08, 2017 (151)
48 URBANLAB ss3646909617 Oct 11, 2018 (152)
49 EGCUT_WGS ss3656582917 Jul 12, 2019 (153)
50 EVA_DECODE ss3688837330 Jul 12, 2019 (153)
51 ACPOP ss3727954165 Jul 12, 2019 (153)
52 EVA ss3747469156 Jul 12, 2019 (153)
53 KHV_HUMAN_GENOMES ss3800470943 Jul 12, 2019 (153)
54 EVA ss3826698662 Apr 25, 2020 (154)
55 EVA ss3836751090 Apr 25, 2020 (154)
56 EVA ss3842163574 Apr 25, 2020 (154)
57 SGDP_PRJ ss3851117521 Apr 25, 2020 (154)
58 KRGDB ss3896465899 Apr 25, 2020 (154)
59 KOGIC ss3946712353 Apr 25, 2020 (154)
60 TOPMED ss4487273516 Apr 25, 2021 (155)
61 TOMMO_GENOMICS ss5148916749 Apr 25, 2021 (155)
62 1000G_HIGH_COVERAGE ss5246164051 Oct 12, 2022 (156)
63 EVA ss5325463614 Oct 12, 2022 (156)
64 HUGCELL_USP ss5446563357 Oct 12, 2022 (156)
65 EVA ss5506227285 Oct 12, 2022 (156)
66 1000G_HIGH_COVERAGE ss5520446337 Oct 12, 2022 (156)
67 SANFORD_IMAGENETICS ss5627655939 Oct 12, 2022 (156)
68 TOMMO_GENOMICS ss5676817907 Oct 12, 2022 (156)
69 YY_MCH ss5801733094 Oct 12, 2022 (156)
70 EVA ss5833411293 Oct 12, 2022 (156)
71 EVA ss5849332439 Oct 12, 2022 (156)
72 EVA ss5912398339 Oct 12, 2022 (156)
73 EVA ss5939504371 Oct 12, 2022 (156)
74 1000Genomes NC_000001.10 - 232147392 Oct 11, 2018 (152)
75 1000Genomes_30x NC_000001.11 - 232011646 Oct 12, 2022 (156)
76 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 232147392 Oct 11, 2018 (152)
77 Genetic variation in the Estonian population NC_000001.10 - 232147392 Oct 11, 2018 (152)
78 The Danish reference pan genome NC_000001.10 - 232147392 Apr 25, 2020 (154)
79 gnomAD - Genomes NC_000001.11 - 232011646 Apr 25, 2021 (155)
80 Genome of the Netherlands Release 5 NC_000001.10 - 232147392 Apr 25, 2020 (154)
81 HapMap NC_000001.11 - 232011646 Apr 25, 2020 (154)
82 KOREAN population from KRGDB NC_000001.10 - 232147392 Apr 25, 2020 (154)
83 Korean Genome Project NC_000001.11 - 232011646 Apr 25, 2020 (154)
84 Northern Sweden NC_000001.10 - 232147392 Jul 12, 2019 (153)
85 Qatari NC_000001.10 - 232147392 Apr 25, 2020 (154)
86 SGDP_PRJ NC_000001.10 - 232147392 Apr 25, 2020 (154)
87 Siberian NC_000001.10 - 232147392 Apr 25, 2020 (154)
88 8.3KJPN NC_000001.10 - 232147392 Apr 25, 2021 (155)
89 14KJPN NC_000001.11 - 232011646 Oct 12, 2022 (156)
90 TopMed NC_000001.11 - 232011646 Apr 25, 2021 (155)
91 UK 10K study - Twins NC_000001.10 - 232147392 Oct 11, 2018 (152)
92 A Vietnamese Genetic Variation Database NC_000001.10 - 232147392 Jul 12, 2019 (153)
93 ALFA NC_000001.11 - 232011646 Apr 25, 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)
rs1176104 Jan 18, 2001 (92)
rs56684561 May 23, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
7705461623 NC_000001.11:232011645:A:G NC_000001.11:232011645:A:G (self)
ss77456164, ss83487778 NC_000001.8:228454126:A:T NC_000001.11:232011645:A:T (self)
ss88007038, ss111928525, ss119244644, ss165390378, ss167561973, ss199742133, ss205275892, ss276259652, ss284246748, ss290755147, ss1585656031 NC_000001.9:230214014:A:T NC_000001.11:232011645:A:T (self)
5941750, 3285805, 2321165, 1929082, 1436320, 3643293, 1239030, 1519426, 3134501, 816440, 6886056, 3285805, 714655, ss218938791, ss230944650, ss238550585, ss555206474, ss648779235, ss976256226, ss1068685966, ss1295071920, ss1426143714, ss1574749150, ss1602364501, ss1645358534, ss1795878848, ss1919477496, ss2020263995, ss2148300086, ss2624644130, ss2698300523, ss2767413330, ss2988623928, ss3343961201, ss3656582917, ss3727954165, ss3747469156, ss3826698662, ss3836751090, ss3851117521, ss3896465899, ss5148916749, ss5325463614, ss5506227285, ss5627655939, ss5833411293, ss5939504371 NC_000001.10:232147391:A:T NC_000001.11:232011645:A:T (self)
7972272, 42621139, 289994, 3090354, 10655011, 50879851, 7705461623, ss2170956492, ss3023892891, ss3646909617, ss3688837330, ss3800470943, ss3842163574, ss3946712353, ss4487273516, ss5246164051, ss5446563357, ss5520446337, ss5676817907, ss5801733094, ss5849332439, ss5912398339 NC_000001.11:232011645:A:T NC_000001.11:232011645:A:T (self)
ss16433677, ss20524003 NT_021973.16:2078380:A:T NC_000001.11:232011645:A:T (self)
ss1098614, ss1620240, ss2448891, ss3976226, ss41084760, ss99295467, ss106639030, ss138172328, ss139038093 NT_167186.1:25665170:A:T NC_000001.11:232011645: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 rs821629

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