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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.

rs12562437

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:3734467 (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
C>A / C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.033602 (4711/140200, GnomAD)
T=0.03318 (2609/78624, PAGE_STUDY)
T=0.03295 (1795/54484, ALFA) (+ 18 more)
T=0.11027 (3116/28258, 14KJPN)
T=0.11187 (1875/16760, 8.3KJPN)
T=0.0532 (341/6404, 1000G_30x)
T=0.0563 (282/5008, 1000G)
T=0.0540 (242/4480, Estonian)
T=0.0402 (155/3854, ALSPAC)
T=0.0318 (118/3708, TWINSUK)
T=0.1467 (428/2918, KOREAN)
T=0.046 (46/998, GoNL)
T=0.181 (138/764, PRJEB37584)
T=0.052 (31/600, NorthernSweden)
T=0.004 (1/234, HapMap)
T=0.056 (12/216, Qatari)
T=0.227 (49/216, Vietnamese)
C=0.47 (32/68, SGDP_PRJ)
T=0.10 (6/58, Ancient Sardinia)
T=0.05 (2/40, GENOME_DK)
C=0.2 (1/4, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TP73 : 3 Prime UTR 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 54484 C=0.96705 A=0.00000, T=0.03295
European Sub 48696 C=0.96497 A=0.00000, T=0.03503
African Sub 2968 C=1.0000 A=0.0000, T=0.0000
African Others Sub 116 C=1.000 A=0.000, T=0.000
African American Sub 2852 C=1.0000 A=0.0000, T=0.0000
Asian Sub 116 C=0.828 A=0.000, T=0.172
East Asian Sub 108 C=0.824 A=0.000, T=0.176
Other Asian Sub 8 C=0.9 A=0.0, T=0.1
Latin American 1 Sub 142 C=1.000 A=0.000, T=0.000
Latin American 2 Sub 592 C=1.000 A=0.000, T=0.000
South Asian Sub 96 C=1.00 A=0.00, T=0.00
Other Sub 1874 C=0.9632 A=0.0000, T=0.0368


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
gnomAD - Genomes Global Study-wide 140200 C=0.966398 T=0.033602
gnomAD - Genomes European Sub 75914 C=0.95883 T=0.04117
gnomAD - Genomes African Sub 42024 C=0.99179 T=0.00821
gnomAD - Genomes American Sub 13660 C=0.98082 T=0.01918
gnomAD - Genomes Ashkenazi Jewish Sub 3320 C=0.9509 T=0.0491
gnomAD - Genomes East Asian Sub 3128 C=0.7625 T=0.2375
gnomAD - Genomes Other Sub 2154 C=0.9661 T=0.0339
The PAGE Study Global Study-wide 78624 C=0.96682 T=0.03318
The PAGE Study AfricanAmerican Sub 32444 C=0.99143 T=0.00857
The PAGE Study Mexican Sub 10810 C=0.98159 T=0.01841
The PAGE Study Asian Sub 8318 C=0.8531 T=0.1469
The PAGE Study PuertoRican Sub 7918 C=0.9883 T=0.0117
The PAGE Study NativeHawaiian Sub 4532 C=0.8817 T=0.1183
The PAGE Study Cuban Sub 4226 C=0.9768 T=0.0232
The PAGE Study Dominican Sub 3828 C=0.9935 T=0.0065
The PAGE Study CentralAmerican Sub 2450 C=0.9796 T=0.0204
The PAGE Study SouthAmerican Sub 1982 C=0.9834 T=0.0166
The PAGE Study NativeAmerican Sub 1260 C=0.9730 T=0.0270
The PAGE Study SouthAsian Sub 856 C=0.952 T=0.048
Allele Frequency Aggregator Total Global 54484 C=0.96705 A=0.00000, T=0.03295
Allele Frequency Aggregator European Sub 48696 C=0.96497 A=0.00000, T=0.03503
Allele Frequency Aggregator African Sub 2968 C=1.0000 A=0.0000, T=0.0000
Allele Frequency Aggregator Other Sub 1874 C=0.9632 A=0.0000, T=0.0368
Allele Frequency Aggregator Latin American 2 Sub 592 C=1.000 A=0.000, T=0.000
Allele Frequency Aggregator Latin American 1 Sub 142 C=1.000 A=0.000, T=0.000
Allele Frequency Aggregator Asian Sub 116 C=0.828 A=0.000, T=0.172
Allele Frequency Aggregator South Asian Sub 96 C=1.00 A=0.00, T=0.00
14KJPN JAPANESE Study-wide 28258 C=0.88973 T=0.11027
8.3KJPN JAPANESE Study-wide 16760 C=0.88813 T=0.11187
1000Genomes_30x Global Study-wide 6404 C=0.9468 T=0.0532
1000Genomes_30x African Sub 1786 C=1.0000 T=0.0000
1000Genomes_30x Europe Sub 1266 C=0.9708 T=0.0292
1000Genomes_30x South Asian Sub 1202 C=0.9684 T=0.0316
1000Genomes_30x East Asian Sub 1170 C=0.7812 T=0.2188
1000Genomes_30x American Sub 980 C=0.990 T=0.010
1000Genomes Global Study-wide 5008 C=0.9437 T=0.0563
1000Genomes African Sub 1322 C=1.0000 T=0.0000
1000Genomes East Asian Sub 1008 C=0.7877 T=0.2123
1000Genomes Europe Sub 1006 C=0.9712 T=0.0288
1000Genomes South Asian Sub 978 C=0.968 T=0.032
1000Genomes American Sub 694 C=0.988 T=0.012
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.9460 T=0.0540
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.9598 T=0.0402
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.9682 T=0.0318
KOREAN population from KRGDB KOREAN Study-wide 2918 C=0.8533 T=0.1467
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.954 T=0.046
CNV burdens in cranial meningiomas Global Study-wide 764 C=0.819 T=0.181
CNV burdens in cranial meningiomas CRM Sub 764 C=0.819 T=0.181
Northern Sweden ACPOP Study-wide 600 C=0.948 T=0.052
HapMap Global Study-wide 234 C=0.996 T=0.004
HapMap African Sub 118 C=1.000 T=0.000
HapMap American Sub 116 C=0.991 T=0.009
Qatari Global Study-wide 216 C=0.944 T=0.056
A Vietnamese Genetic Variation Database Global Study-wide 216 C=0.773 T=0.227
SGDP_PRJ Global Study-wide 68 C=0.47 T=0.53
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 58 C=0.90 T=0.10
The Danish reference pan genome Danish Study-wide 40 C=0.95 T=0.05
Siberian Global Study-wide 4 C=0.2 T=0.8
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.3734467C>A
GRCh38.p14 chr 1 NC_000001.11:g.3734467C>T
GRCh37.p13 chr 1 NC_000001.10:g.3651031C>A
GRCh37.p13 chr 1 NC_000001.10:g.3651031C>T
TP73 RefSeqGene NG_017035.2:g.86903C>A
TP73 RefSeqGene NG_017035.2:g.86903C>T
Gene: TP73, tumor protein p73 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TP73 transcript variant 1 NM_005427.4:c.*1388= N/A 3 Prime UTR Variant
TP73 transcript variant 7 NM_001204191.2:c.*1388= N/A 3 Prime UTR Variant
TP73 transcript variant 6 NM_001204190.2:c.*1388= N/A 3 Prime UTR Variant
TP73 transcript variant 3 NM_001126241.3:c.*1705= N/A 3 Prime UTR Variant
TP73 transcript variant 2 NM_001126240.3:c.*1388= N/A 3 Prime UTR Variant
TP73 transcript variant 10 NM_001204186.2:c.*1705= N/A 3 Prime UTR Variant
TP73 transcript variant 9 NM_001204185.2:c.*1722= N/A 3 Prime UTR Variant
TP73 transcript variant 8 NM_001204184.2:c.*1705= N/A 3 Prime UTR Variant
TP73 transcript variant 13 NM_001204192.2:c.*1388= N/A 3 Prime UTR Variant
TP73 transcript variant 4 NM_001126242.3:c.*1722= N/A 3 Prime UTR Variant
TP73 transcript variant 5 NM_001204189.2:c.*1705= N/A 3 Prime UTR Variant
TP73 transcript variant 12 NM_001204188.2:c.*1388= N/A 3 Prime UTR Variant
TP73 transcript variant 11 NM_001204187.2:c.*1388= N/A 3 Prime UTR Variant
TP73 transcript variant X1 XM_047429521.1:c.*1388= N/A 3 Prime UTR Variant
TP73 transcript variant X2 XM_047429524.1:c.*1388= N/A 3 Prime UTR 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 C= A T
GRCh38.p14 chr 1 NC_000001.11:g.3734467= NC_000001.11:g.3734467C>A NC_000001.11:g.3734467C>T
GRCh37.p13 chr 1 NC_000001.10:g.3651031= NC_000001.10:g.3651031C>A NC_000001.10:g.3651031C>T
TP73 RefSeqGene NG_017035.2:g.86903= NG_017035.2:g.86903C>A NG_017035.2:g.86903C>T
TP73 transcript variant 1 NM_005427.4:c.*1388= NM_005427.4:c.*1388C>A NM_005427.4:c.*1388C>T
TP73 transcript variant 1 NM_005427.3:c.*1388= NM_005427.3:c.*1388C>A NM_005427.3:c.*1388C>T
TP73 transcript variant 2 NM_001126240.3:c.*1388= NM_001126240.3:c.*1388C>A NM_001126240.3:c.*1388C>T
TP73 transcript variant 2 NM_001126240.2:c.*1388= NM_001126240.2:c.*1388C>A NM_001126240.2:c.*1388C>T
TP73 transcript variant 3 NM_001126241.3:c.*1705= NM_001126241.3:c.*1705C>A NM_001126241.3:c.*1705C>T
TP73 transcript variant 3 NM_001126241.2:c.*1705= NM_001126241.2:c.*1705C>A NM_001126241.2:c.*1705C>T
TP73 transcript variant 4 NM_001126242.3:c.*1722= NM_001126242.3:c.*1722C>A NM_001126242.3:c.*1722C>T
TP73 transcript variant 4 NM_001126242.2:c.*1722= NM_001126242.2:c.*1722C>A NM_001126242.2:c.*1722C>T
TP73 transcript variant 8 NM_001204184.2:c.*1705= NM_001204184.2:c.*1705C>A NM_001204184.2:c.*1705C>T
TP73 transcript variant 8 NM_001204184.1:c.*1705= NM_001204184.1:c.*1705C>A NM_001204184.1:c.*1705C>T
TP73 transcript variant 9 NM_001204185.2:c.*1722= NM_001204185.2:c.*1722C>A NM_001204185.2:c.*1722C>T
TP73 transcript variant 9 NM_001204185.1:c.*1722= NM_001204185.1:c.*1722C>A NM_001204185.1:c.*1722C>T
TP73 transcript variant 13 NM_001204192.2:c.*1388= NM_001204192.2:c.*1388C>A NM_001204192.2:c.*1388C>T
TP73 transcript variant 13 NM_001204192.1:c.*1388= NM_001204192.1:c.*1388C>A NM_001204192.1:c.*1388C>T
TP73 transcript variant 11 NM_001204187.2:c.*1388= NM_001204187.2:c.*1388C>A NM_001204187.2:c.*1388C>T
TP73 transcript variant 11 NM_001204187.1:c.*1388= NM_001204187.1:c.*1388C>A NM_001204187.1:c.*1388C>T
TP73 transcript variant 12 NM_001204188.2:c.*1388= NM_001204188.2:c.*1388C>A NM_001204188.2:c.*1388C>T
TP73 transcript variant 12 NM_001204188.1:c.*1388= NM_001204188.1:c.*1388C>A NM_001204188.1:c.*1388C>T
TP73 transcript variant 6 NM_001204190.2:c.*1388= NM_001204190.2:c.*1388C>A NM_001204190.2:c.*1388C>T
TP73 transcript variant 6 NM_001204190.1:c.*1388= NM_001204190.1:c.*1388C>A NM_001204190.1:c.*1388C>T
TP73 transcript variant 7 NM_001204191.2:c.*1388= NM_001204191.2:c.*1388C>A NM_001204191.2:c.*1388C>T
TP73 transcript variant 7 NM_001204191.1:c.*1388= NM_001204191.1:c.*1388C>A NM_001204191.1:c.*1388C>T
TP73 transcript variant 10 NM_001204186.2:c.*1705= NM_001204186.2:c.*1705C>A NM_001204186.2:c.*1705C>T
TP73 transcript variant 10 NM_001204186.1:c.*1705= NM_001204186.1:c.*1705C>A NM_001204186.1:c.*1705C>T
TP73 transcript variant 5 NM_001204189.2:c.*1705= NM_001204189.2:c.*1705C>A NM_001204189.2:c.*1705C>T
TP73 transcript variant 5 NM_001204189.1:c.*1705= NM_001204189.1:c.*1705C>A NM_001204189.1:c.*1705C>T
TP73 transcript variant X2 XM_047429524.1:c.*1388= XM_047429524.1:c.*1388C>A XM_047429524.1:c.*1388C>T
TP73 transcript variant X1 XM_047429521.1:c.*1388= XM_047429521.1:c.*1388C>A XM_047429521.1:c.*1388C>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#.

66 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 CSHL-HAPMAP ss19833416 Feb 28, 2004 (120)
2 ABI ss44032525 Mar 14, 2006 (126)
3 BGI ss105114821 Dec 01, 2009 (131)
4 ENSEMBL ss161248968 Dec 01, 2009 (131)
5 1000GENOMES ss230403862 Jul 14, 2010 (132)
6 1000GENOMES ss238122823 Jul 15, 2010 (132)
7 GMI ss275691245 May 04, 2012 (137)
8 TISHKOFF ss553734123 Apr 25, 2013 (138)
9 SSMP ss647535909 Apr 25, 2013 (138)
10 EVA-GONL ss974795653 Aug 21, 2014 (142)
11 JMKIDD_LAB ss1067626805 Aug 21, 2014 (142)
12 1000GENOMES ss1289448759 Aug 21, 2014 (142)
13 DDI ss1425692714 Apr 01, 2015 (144)
14 EVA_GENOME_DK ss1573859811 Apr 01, 2015 (144)
15 EVA_DECODE ss1584154465 Apr 01, 2015 (144)
16 EVA_UK10K_ALSPAC ss1599425886 Apr 01, 2015 (144)
17 EVA_UK10K_TWINSUK ss1642419919 Apr 01, 2015 (144)
18 WEILL_CORNELL_DGM ss1917991265 Feb 12, 2016 (147)
19 ILLUMINA ss1945982738 Feb 12, 2016 (147)
20 ILLUMINA ss1958234642 Feb 12, 2016 (147)
21 JJLAB ss2019511709 Sep 14, 2016 (149)
22 USC_VALOUEV ss2147502139 Dec 20, 2016 (150)
23 HUMAN_LONGEVITY ss2159568736 Dec 20, 2016 (150)
24 ILLUMINA ss2632468597 Nov 08, 2017 (151)
25 GRF ss2697396105 Nov 08, 2017 (151)
26 ILLUMINA ss2710664055 Nov 08, 2017 (151)
27 GNOMAD ss2750964594 Nov 08, 2017 (151)
28 SWEGEN ss2986200166 Nov 08, 2017 (151)
29 ILLUMINA ss3021047531 Nov 08, 2017 (151)
30 CSHL ss3343288585 Nov 08, 2017 (151)
31 ILLUMINA ss3625523860 Oct 11, 2018 (152)
32 ILLUMINA ss3644478597 Oct 11, 2018 (152)
33 ILLUMINA ss3651370181 Oct 11, 2018 (152)
34 EGCUT_WGS ss3654301293 Jul 12, 2019 (153)
35 EVA_DECODE ss3686045824 Jul 12, 2019 (153)
36 ILLUMINA ss3724990806 Jul 12, 2019 (153)
37 ACPOP ss3726739381 Jul 12, 2019 (153)
38 ILLUMINA ss3744041041 Jul 12, 2019 (153)
39 EVA ss3745754336 Jul 12, 2019 (153)
40 PAGE_CC ss3770780753 Jul 12, 2019 (153)
41 KHV_HUMAN_GENOMES ss3798776109 Jul 12, 2019 (153)
42 EVA ss3825551208 Apr 25, 2020 (154)
43 EVA ss3825993646 Apr 25, 2020 (154)
44 SGDP_PRJ ss3848068128 Apr 25, 2020 (154)
45 KRGDB ss3892929439 Apr 25, 2020 (154)
46 EVA ss3984451120 Apr 25, 2021 (155)
47 EVA ss3984774902 Apr 25, 2021 (155)
48 TOPMED ss4437282924 Apr 25, 2021 (155)
49 TOPMED ss4437282925 Apr 25, 2021 (155)
50 TOMMO_GENOMICS ss5142198622 Apr 25, 2021 (155)
51 EVA ss5237258751 Apr 25, 2021 (155)
52 1000G_HIGH_COVERAGE ss5240965789 Oct 13, 2022 (156)
53 EVA ss5316368946 Oct 13, 2022 (156)
54 HUGCELL_USP ss5442191749 Oct 13, 2022 (156)
55 1000G_HIGH_COVERAGE ss5512630334 Oct 13, 2022 (156)
56 SANFORD_IMAGENETICS ss5624194497 Oct 13, 2022 (156)
57 SANFORD_IMAGENETICS ss5624807161 Oct 13, 2022 (156)
58 TOMMO_GENOMICS ss5666411467 Oct 13, 2022 (156)
59 YY_MCH ss5800271039 Oct 13, 2022 (156)
60 EVA ss5831458677 Oct 13, 2022 (156)
61 EVA ss5847151211 Oct 13, 2022 (156)
62 EVA ss5847522753 Oct 13, 2022 (156)
63 EVA ss5848758845 Oct 13, 2022 (156)
64 EVA ss5906808053 Oct 13, 2022 (156)
65 EVA ss5936631884 Oct 13, 2022 (156)
66 EVA ss5979260693 Oct 13, 2022 (156)
67 1000Genomes NC_000001.10 - 3651031 Oct 11, 2018 (152)
68 1000Genomes_30x NC_000001.11 - 3734467 Oct 13, 2022 (156)
69 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 3651031 Oct 11, 2018 (152)
70 Genetic variation in the Estonian population NC_000001.10 - 3651031 Oct 11, 2018 (152)
71 The Danish reference pan genome NC_000001.10 - 3651031 Apr 25, 2020 (154)
72 gnomAD - Genomes NC_000001.11 - 3734467 Apr 25, 2021 (155)
73 Genome of the Netherlands Release 5 NC_000001.10 - 3651031 Apr 25, 2020 (154)
74 HapMap NC_000001.11 - 3734467 Apr 25, 2020 (154)
75 KOREAN population from KRGDB NC_000001.10 - 3651031 Apr 25, 2020 (154)
76 Northern Sweden NC_000001.10 - 3651031 Jul 12, 2019 (153)
77 The PAGE Study NC_000001.11 - 3734467 Jul 12, 2019 (153)
78 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 3651031 Apr 25, 2021 (155)
79 CNV burdens in cranial meningiomas NC_000001.10 - 3651031 Apr 25, 2021 (155)
80 Qatari NC_000001.10 - 3651031 Apr 25, 2020 (154)
81 SGDP_PRJ NC_000001.10 - 3651031 Apr 25, 2020 (154)
82 Siberian NC_000001.10 - 3651031 Apr 25, 2020 (154)
83 8.3KJPN NC_000001.10 - 3651031 Apr 25, 2021 (155)
84 14KJPN NC_000001.11 - 3734467 Oct 13, 2022 (156)
85 TopMed

Submission ignored due to conflicting rows:
Row 889259 (NC_000001.11:3734466:C:A 1/264690)
Row 889260 (NC_000001.11:3734466:C:T 8916/264690)

- Apr 25, 2021 (155)
86 TopMed

Submission ignored due to conflicting rows:
Row 889259 (NC_000001.11:3734466:C:A 1/264690)
Row 889260 (NC_000001.11:3734466:C:T 8916/264690)

- Apr 25, 2021 (155)
87 UK 10K study - Twins NC_000001.10 - 3651031 Oct 11, 2018 (152)
88 A Vietnamese Genetic Variation Database NC_000001.10 - 3651031 Jul 12, 2019 (153)
89 ALFA NC_000001.11 - 3734467 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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
12291857371, ss4437282924 NC_000001.11:3734466:C:A NC_000001.11:3734466:C:A (self)
ss275691245, ss1584154465 NC_000001.9:3640890:C:T NC_000001.11:3734466:C:T (self)
116695, 52009, 39541, 1367045, 22323, 106833, 24246, 829, 420, 33195, 85108, 18493, 167929, 52009, 10948, ss230403862, ss238122823, ss553734123, ss647535909, ss974795653, ss1067626805, ss1289448759, ss1425692714, ss1573859811, ss1599425886, ss1642419919, ss1917991265, ss1945982738, ss1958234642, ss2019511709, ss2147502139, ss2632468597, ss2697396105, ss2710664055, ss2750964594, ss2986200166, ss3021047531, ss3343288585, ss3625523860, ss3644478597, ss3651370181, ss3654301293, ss3726739381, ss3744041041, ss3745754336, ss3825551208, ss3825993646, ss3848068128, ss3892929439, ss3984451120, ss3984774902, ss5142198622, ss5237258751, ss5316368946, ss5624194497, ss5624807161, ss5831458677, ss5847151211, ss5847522753, ss5936631884, ss5979260693 NC_000001.10:3651030:C:T NC_000001.11:3734466:C:T (self)
156269, 844999, 2703, 2222, 248571, 12291857371, ss2159568736, ss3686045824, ss3724990806, ss3770780753, ss3798776109, ss4437282925, ss5240965789, ss5442191749, ss5512630334, ss5666411467, ss5800271039, ss5848758845, ss5906808053 NC_000001.11:3734466:C:T NC_000001.11:3734466:C:T (self)
ss19833416 NT_004321.15:957805:C:T NC_000001.11:3734466:C:T (self)
ss44032525, ss105114821, ss161248968 NT_004350.19:3129662:C:T NC_000001.11:3734466:C:T (self)
Removed from this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Destination RSIDs
ss2321723710 NC_000001.10:3651030:C:A NC_000001.11:3734466:C:A
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 rs12562437

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