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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.

rs2760321

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr1:3631572 (GRCh38.p13) 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
T=0.140428 (37170/264690, TOPMED)
T=0.129661 (31981/246650, GnomAD_exome)
T=0.142053 (19923/140250, GnomAD) (+ 23 more)
T=0.127313 (15068/118354, ExAC)
T=0.15633 (15029/96138, ALFA)
T=0.11136 (8741/78496, PAGE_STUDY)
T=0.00024 (4/16754, 8.3KJPN)
T=0.14952 (1944/13002, GO-ESP)
T=0.0938 (470/5008, 1000G)
T=0.1158 (519/4480, Estonian)
T=0.1694 (653/3854, ALSPAC)
T=0.1731 (642/3708, TWINSUK)
T=0.0017 (5/2926, KOREAN)
T=0.0926 (193/2084, HGDP_Stanford)
T=0.0005 (1/1832, Korea1K)
T=0.1269 (229/1804, HapMap)
T=0.157 (157/998, GoNL)
T=0.010 (6/616, Vietnamese)
T=0.145 (87/600, NorthernSweden)
T=0.092 (50/546, SGDP_PRJ)
C=0.212 (113/534, MGP)
T=0.115 (35/304, FINRISK)
T=0.204 (44/216, Qatari)
T=0.04 (2/56, Siberian)
T=0.40 (20/50, Ancient Sardinia)
T=0.17 (7/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
WRAP73 : Synonymous Variant
Publications
0 citations
Genomic View
See rs on genome
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.p13 chr 1 NC_000001.11:g.3631572T>C
GRCh37.p13 chr 1 NC_000001.10:g.3548136T>C
WRAP73 RefSeqGene NG_033937.1:g.23536A>G
Gene: WRAP73, WD repeat containing, antisense to TP73 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
WRAP73 transcript NM_017818.4:c.1134A>G A [GCA] > A [GCG] Coding Sequence Variant
WD repeat-containing protein WRAP73 NP_060288.3:p.Ala378= A (Ala) > A (Ala) Synonymous Variant
WRAP73 transcript variant X1 XM_017001387.2:c.1113A>G A [GCA] > A [GCG] Coding Sequence Variant
WD repeat-containing protein WRAP73 isoform X1 XP_016856876.1:p.Ala371= A (Ala) > A (Ala) Synonymous Variant
WRAP73 transcript variant X2 XM_005244754.2:c.999A>G A [GCA] > A [GCG] Coding Sequence Variant
WD repeat-containing protein WRAP73 isoform X2 XP_005244811.1:p.Ala333= A (Ala) > A (Ala) Synonymous Variant
WRAP73 transcript variant X3 XR_946661.3:n.1208A>G N/A Non Coding 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

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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 96138 T=0.15633 C=0.84367
European Sub 76372 T=0.16384 C=0.83616
African Sub 5138 T=0.1300 C=0.8700
African Others Sub 178 T=0.118 C=0.882
African American Sub 4960 T=0.1304 C=0.8696
Asian Sub 276 T=0.014 C=0.986
East Asian Sub 206 T=0.010 C=0.990
Other Asian Sub 70 T=0.03 C=0.97
Latin American 1 Sub 598 T=0.129 C=0.871
Latin American 2 Sub 1242 T=0.1288 C=0.8712
South Asian Sub 4962 T=0.0732 C=0.9268
Other Sub 7550 T=0.1648 C=0.8352


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=0.140428 C=0.859572
gnomAD - Exomes Global Study-wide 246650 T=0.129661 C=0.870339
gnomAD - Exomes European Sub 131684 T=0.155068 C=0.844932
gnomAD - Exomes Asian Sub 48746 T=0.04739 C=0.95261
gnomAD - Exomes American Sub 34404 T=0.12882 C=0.87118
gnomAD - Exomes African Sub 15790 T=0.12362 C=0.87638
gnomAD - Exomes Ashkenazi Jewish Sub 9998 T=0.1950 C=0.8050
gnomAD - Exomes Other Sub 6028 T=0.1521 C=0.8479
gnomAD - Genomes Global Study-wide 140250 T=0.142053 C=0.857947
gnomAD - Genomes European Sub 75944 T=0.15735 C=0.84265
gnomAD - Genomes African Sub 42036 T=0.12446 C=0.87554
gnomAD - Genomes American Sub 13662 T=0.12582 C=0.87418
gnomAD - Genomes Ashkenazi Jewish Sub 3324 T=0.2031 C=0.7969
gnomAD - Genomes East Asian Sub 3130 T=0.0045 C=0.9955
gnomAD - Genomes Other Sub 2154 T=0.1546 C=0.8454
ExAC Global Study-wide 118354 T=0.127313 C=0.872687
ExAC Europe Sub 71298 T=0.15538 C=0.84462
ExAC Asian Sub 24880 T=0.04695 C=0.95305
ExAC American Sub 11386 T=0.13069 C=0.86931
ExAC African Sub 9926 T=0.1229 C=0.8771
ExAC Other Sub 864 T=0.132 C=0.868
The PAGE Study Global Study-wide 78496 T=0.11136 C=0.88864
The PAGE Study AfricanAmerican Sub 32362 T=0.12657 C=0.87343
The PAGE Study Mexican Sub 10804 T=0.13143 C=0.86857
The PAGE Study Asian Sub 8300 T=0.0039 C=0.9961
The PAGE Study PuertoRican Sub 7914 T=0.1309 C=0.8691
The PAGE Study NativeHawaiian Sub 4524 T=0.0568 C=0.9432
The PAGE Study Cuban Sub 4228 T=0.1474 C=0.8526
The PAGE Study Dominican Sub 3820 T=0.1212 C=0.8788
The PAGE Study CentralAmerican Sub 2450 T=0.1237 C=0.8763
The PAGE Study SouthAmerican Sub 1980 T=0.1338 C=0.8662
The PAGE Study NativeAmerican Sub 1260 T=0.1556 C=0.8444
The PAGE Study SouthAsian Sub 854 T=0.059 C=0.941
8.3KJPN JAPANESE Study-wide 16754 T=0.00024 C=0.99976
GO Exome Sequencing Project Global Study-wide 13002 T=0.14952 C=0.85048
GO Exome Sequencing Project European American Sub 8600 T=0.1627 C=0.8373
GO Exome Sequencing Project African American Sub 4402 T=0.1238 C=0.8762
1000Genomes Global Study-wide 5008 T=0.0938 C=0.9062
1000Genomes African Sub 1322 T=0.1074 C=0.8926
1000Genomes East Asian Sub 1008 T=0.0050 C=0.9950
1000Genomes Europe Sub 1006 T=0.1640 C=0.8360
1000Genomes South Asian Sub 978 T=0.052 C=0.948
1000Genomes American Sub 694 T=0.154 C=0.846
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.1158 C=0.8842
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.1694 C=0.8306
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.1731 C=0.8269
KOREAN population from KRGDB KOREAN Study-wide 2926 T=0.0017 C=0.9983
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 T=0.0926 C=0.9074
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 T=0.006 C=0.994
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 T=0.087 C=0.913
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 T=0.157 C=0.843
HGDP-CEPH-db Supplement 1 Europe Sub 320 T=0.169 C=0.831
HGDP-CEPH-db Supplement 1 Africa Sub 242 T=0.062 C=0.938
HGDP-CEPH-db Supplement 1 America Sub 216 T=0.069 C=0.931
HGDP-CEPH-db Supplement 1 Oceania Sub 72 T=0.21 C=0.79
Korean Genome Project KOREAN Study-wide 1832 T=0.0005 C=0.9995
HapMap Global Study-wide 1804 T=0.1269 C=0.8731
HapMap American Sub 766 T=0.095 C=0.905
HapMap African Sub 690 T=0.174 C=0.826
HapMap Europe Sub 176 T=0.199 C=0.801
HapMap Asian Sub 172 T=0.006 C=0.994
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.157 C=0.843
A Vietnamese Genetic Variation Database Global Study-wide 616 T=0.010 C=0.990
Northern Sweden ACPOP Study-wide 600 T=0.145 C=0.855
SGDP_PRJ Global Study-wide 546 T=0.092 C=0.908
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 T=0.788 C=0.212
FINRISK Finnish from FINRISK project Study-wide 304 T=0.115 C=0.885
Qatari Global Study-wide 216 T=0.204 C=0.796
Siberian Global Study-wide 56 T=0.04 C=0.96
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 50 T=0.40 C=0.60
The Danish reference pan genome Danish Study-wide 40 T=0.17 C=0.82
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.p13 chr 1 NC_000001.11:g.3631572= NC_000001.11:g.3631572T>C
GRCh37.p13 chr 1 NC_000001.10:g.3548136= NC_000001.10:g.3548136T>C
WRAP73 RefSeqGene NG_033937.1:g.23536= NG_033937.1:g.23536A>G
WRAP73 transcript NM_017818.4:c.1134= NM_017818.4:c.1134A>G
WRAP73 transcript NM_017818.3:c.1134= NM_017818.3:c.1134A>G
WRAP73 transcript variant X3 XR_946661.3:n.1208= XR_946661.3:n.1208A>G
WRAP73 transcript variant X1 XM_017001387.2:c.1113= XM_017001387.2:c.1113A>G
WRAP73 transcript variant X2 XM_005244754.2:c.999= XM_005244754.2:c.999A>G
WRAP73 transcript variant X2 XM_005244754.1:c.999= XM_005244754.1:c.999A>G
WD repeat-containing protein WRAP73 NP_060288.3:p.Ala378= NP_060288.3:p.Ala378=
WD repeat-containing protein WRAP73 isoform X1 XP_016856876.1:p.Ala371= XP_016856876.1:p.Ala371=
WD repeat-containing protein WRAP73 isoform X2 XP_005244811.1:p.Ala333= XP_005244811.1:p.Ala333=
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#.

120 SubSNP, 26 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss3897985 Sep 28, 2001 (100)
2 CGAP-GAI ss4321013 Jan 04, 2002 (102)
3 SC_JCM ss6232547 Feb 20, 2003 (111)
4 WI_SSAHASNP ss6396663 Feb 20, 2003 (111)
5 SC_SNP ss12992682 Dec 05, 2003 (119)
6 CGAP-GAI ss16253056 Feb 27, 2004 (120)
7 CSHL-HAPMAP ss16429457 Feb 27, 2004 (120)
8 SSAHASNP ss20484820 Apr 05, 2004 (121)
9 PERLEGEN ss23157527 Sep 20, 2004 (123)
10 ILLUMINA ss67271802 Nov 30, 2006 (127)
11 ILLUMINA ss67672566 Nov 30, 2006 (127)
12 ILLUMINA ss68211610 Dec 12, 2006 (127)
13 ILLUMINA ss70750269 May 25, 2008 (130)
14 ILLUMINA ss71322591 May 17, 2007 (127)
15 ILLUMINA ss75862628 Dec 06, 2007 (129)
16 HGSV ss78711856 Dec 06, 2007 (129)
17 KRIBB_YJKIM ss84078467 Dec 15, 2007 (130)
18 HGSV ss85002000 Dec 15, 2007 (130)
19 CORNELL ss86238958 Mar 23, 2008 (129)
20 HUMANGENOME_JCVI ss97915363 Feb 05, 2009 (130)
21 BGI ss105114661 Dec 01, 2009 (131)
22 1000GENOMES ss109965650 Jan 24, 2009 (130)
23 ILLUMINA-UK ss118452478 Feb 14, 2009 (130)
24 ENSEMBL ss139864187 Dec 01, 2009 (131)
25 ILLUMINA ss154232615 Dec 01, 2009 (131)
26 GMI ss154558772 Dec 01, 2009 (131)
27 ILLUMINA ss159409081 Dec 01, 2009 (131)
28 SEATTLESEQ ss159695833 Dec 01, 2009 (131)
29 COMPLETE_GENOMICS ss163735369 Jul 04, 2010 (132)
30 ILLUMINA ss173454819 Jul 04, 2010 (132)
31 BUSHMAN ss197922321 Jul 04, 2010 (132)
32 BCM-HGSC-SUB ss205508057 Jul 04, 2010 (132)
33 1000GENOMES ss217314384 Jul 14, 2010 (132)
34 1000GENOMES ss217390826 Jul 14, 2010 (132)
35 1000GENOMES ss217392058 Jul 14, 2010 (132)
36 1000GENOMES ss217399965 Jul 14, 2010 (132)
37 1000GENOMES ss217405793 Jul 14, 2010 (132)
38 1000GENOMES ss217410461 Jul 14, 2010 (132)
39 1000GENOMES ss217410944 Jul 14, 2010 (132)
40 1000GENOMES ss218202387 Jul 14, 2010 (132)
41 1000GENOMES ss230403527 Jul 14, 2010 (132)
42 1000GENOMES ss238122487 Jul 15, 2010 (132)
43 BL ss252879315 May 09, 2011 (134)
44 GMI ss275690953 May 04, 2012 (137)
45 GMI ss283990797 Apr 25, 2013 (138)
46 PJP ss290498018 May 09, 2011 (134)
47 NHLBI-ESP ss341927344 May 09, 2011 (134)
48 1000GENOMES ss489716381 May 04, 2012 (137)
49 CLINSEQ_SNP ss491582820 May 04, 2012 (137)
50 TISHKOFF ss553733206 Apr 25, 2013 (138)
51 SSMP ss647535175 Apr 25, 2013 (138)
52 ILLUMINA ss832920762 Jul 12, 2019 (153)
53 EVA-GONL ss974794651 Aug 21, 2014 (142)
54 JMKIDD_LAB ss1067415149 Aug 21, 2014 (142)
55 JMKIDD_LAB ss1067626224 Aug 21, 2014 (142)
56 1000GENOMES ss1289444940 Aug 21, 2014 (142)
57 DDI ss1425692421 Apr 01, 2015 (144)
58 EVA_GENOME_DK ss1573859458 Apr 01, 2015 (144)
59 EVA_FINRISK ss1584004011 Apr 01, 2015 (144)
60 EVA_DECODE ss1584153592 Apr 01, 2015 (144)
61 EVA_UK10K_ALSPAC ss1599424084 Apr 01, 2015 (144)
62 EVA_UK10K_TWINSUK ss1642418117 Apr 01, 2015 (144)
63 EVA_EXAC ss1685260178 Apr 01, 2015 (144)
64 EVA_MGP ss1710885465 Apr 01, 2015 (144)
65 EVA_SVP ss1712306657 Apr 01, 2015 (144)
66 HAMMER_LAB ss1793782489 Sep 08, 2015 (146)
67 WEILL_CORNELL_DGM ss1917990139 Feb 12, 2016 (147)
68 ILLUMINA ss1958234494 Feb 12, 2016 (147)
69 GENOMED ss1966671079 Jul 19, 2016 (147)
70 JJLAB ss2019511229 Sep 14, 2016 (149)
71 USC_VALOUEV ss2147501564 Dec 20, 2016 (150)
72 HUMAN_LONGEVITY ss2159561008 Dec 20, 2016 (150)
73 TOPMED ss2321716112 Dec 20, 2016 (150)
74 SYSTEMSBIOZJU ss2624271452 Nov 08, 2017 (151)
75 GRF ss2697395471 Nov 08, 2017 (151)
76 GNOMAD ss2731054482 Nov 08, 2017 (151)
77 GNOMAD ss2746194368 Nov 08, 2017 (151)
78 GNOMAD ss2750954454 Nov 08, 2017 (151)
79 SWEGEN ss2986198749 Nov 08, 2017 (151)
80 ILLUMINA ss3021047390 Nov 08, 2017 (151)
81 BIOINF_KMB_FNS_UNIBA ss3023519243 Nov 08, 2017 (151)
82 TOPMED ss3067087364 Nov 08, 2017 (151)
83 CSHL ss3343288065 Nov 08, 2017 (151)
84 ILLUMINA ss3637733669 Oct 11, 2018 (152)
85 ILLUMINA ss3638888245 Oct 11, 2018 (152)
86 ILLUMINA ss3639756999 Oct 11, 2018 (152)
87 ILLUMINA ss3642747880 Oct 11, 2018 (152)
88 ILLUMINA ss3643810922 Oct 11, 2018 (152)
89 OMUKHERJEE_ADBS ss3646220098 Oct 11, 2018 (152)
90 URBANLAB ss3646586412 Oct 11, 2018 (152)
91 ILLUMINA ss3651370036 Oct 11, 2018 (152)
92 EGCUT_WGS ss3654299820 Jul 12, 2019 (153)
93 EVA_DECODE ss3686043985 Jul 12, 2019 (153)
94 ILLUMINA ss3724990704 Jul 12, 2019 (153)
95 ACPOP ss3726738590 Jul 12, 2019 (153)
96 EVA ss3745753095 Jul 12, 2019 (153)
97 PAGE_CC ss3770780656 Jul 12, 2019 (153)
98 PACBIO ss3783308410 Jul 12, 2019 (153)
99 PACBIO ss3788985321 Jul 12, 2019 (153)
100 PACBIO ss3793857949 Jul 12, 2019 (153)
101 KHV_HUMAN_GENOMES ss3798774823 Jul 12, 2019 (153)
102 EVA ss3823550230 Apr 25, 2020 (154)
103 EVA ss3825551130 Apr 25, 2020 (154)
104 EVA ss3825993226 Apr 25, 2020 (154)
105 EVA ss3836383723 Apr 25, 2020 (154)
106 EVA ss3841787872 Apr 25, 2020 (154)
107 HGDP ss3847322533 Apr 25, 2020 (154)
108 SGDP_PRJ ss3848065857 Apr 25, 2020 (154)
109 KRGDB ss3892926825 Apr 25, 2020 (154)
110 KOGIC ss3943689071 Apr 25, 2020 (154)
111 FSA-LAB ss3983912913 Apr 25, 2021 (155)
112 FSA-LAB ss3983912914 Apr 25, 2021 (155)
113 EVA ss3984774868 Apr 25, 2021 (155)
114 EVA ss3986008141 Apr 25, 2021 (155)
115 EVA ss3986095080 Apr 25, 2021 (155)
116 EVA ss4016890026 Apr 25, 2021 (155)
117 TOPMED ss4437253932 Apr 25, 2021 (155)
118 TOMMO_GENOMICS ss5142194374 Apr 25, 2021 (155)
119 EVA ss5236863339 Apr 25, 2021 (155)
120 EVA ss5237158755 Apr 25, 2021 (155)
121 1000Genomes NC_000001.10 - 3548136 Oct 11, 2018 (152)
122 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 3548136 Oct 11, 2018 (152)
123 Genetic variation in the Estonian population NC_000001.10 - 3548136 Oct 11, 2018 (152)
124 ExAC NC_000001.10 - 3548136 Oct 11, 2018 (152)
125 FINRISK NC_000001.10 - 3548136 Apr 25, 2020 (154)
126 The Danish reference pan genome NC_000001.10 - 3548136 Apr 25, 2020 (154)
127 gnomAD - Genomes NC_000001.11 - 3631572 Apr 25, 2021 (155)
128 gnomAD - Exomes NC_000001.10 - 3548136 Jul 12, 2019 (153)
129 GO Exome Sequencing Project NC_000001.10 - 3548136 Oct 11, 2018 (152)
130 Genome of the Netherlands Release 5 NC_000001.10 - 3548136 Apr 25, 2020 (154)
131 HGDP-CEPH-db Supplement 1 NC_000001.9 - 3537996 Apr 25, 2020 (154)
132 HapMap NC_000001.11 - 3631572 Apr 25, 2020 (154)
133 KOREAN population from KRGDB NC_000001.10 - 3548136 Apr 25, 2020 (154)
134 Korean Genome Project NC_000001.11 - 3631572 Apr 25, 2020 (154)
135 Medical Genome Project healthy controls from Spanish population NC_000001.10 - 3548136 Apr 25, 2020 (154)
136 Northern Sweden NC_000001.10 - 3548136 Jul 12, 2019 (153)
137 The PAGE Study NC_000001.11 - 3631572 Jul 12, 2019 (153)
138 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 3548136 Apr 25, 2021 (155)
139 Qatari NC_000001.10 - 3548136 Apr 25, 2020 (154)
140 SGDP_PRJ NC_000001.10 - 3548136 Apr 25, 2020 (154)
141 Siberian NC_000001.10 - 3548136 Apr 25, 2020 (154)
142 8.3KJPN NC_000001.10 - 3548136 Apr 25, 2021 (155)
143 TopMed NC_000001.11 - 3631572 Apr 25, 2021 (155)
144 UK 10K study - Twins NC_000001.10 - 3548136 Oct 11, 2018 (152)
145 A Vietnamese Genetic Variation Database NC_000001.10 - 3548136 Jul 12, 2019 (153)
146 ALFA NC_000001.11 - 3631572 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)
rs59786710 May 25, 2008 (130)
rs117829860 Aug 16, 2010 (132)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss78711856, ss85002000, ss3638888245, ss3639756999, ss3643810922 NC_000001.8:3571292:T:C NC_000001.11:3631571:T:C (self)
425, ss109965650, ss118452478, ss163735369, ss197922321, ss205508057, ss217314384, ss217390826, ss217392058, ss217399965, ss217405793, ss217410461, ss217410944, ss252879315, ss275690953, ss283990797, ss290498018, ss491582820, ss1584153592, ss1712306657, ss3642747880, ss3847322533 NC_000001.9:3537995:T:C NC_000001.11:3631571:T:C (self)
112763, 50063, 38068, 4436399, 472, 1366692, 69378, 8964, 21470, 104219, 2217, 23455, 795, 32069, 82837, 17918, 163681, 50063, 10465, ss218202387, ss230403527, ss238122487, ss341927344, ss489716381, ss553733206, ss647535175, ss832920762, ss974794651, ss1067415149, ss1067626224, ss1289444940, ss1425692421, ss1573859458, ss1584004011, ss1599424084, ss1642418117, ss1685260178, ss1710885465, ss1793782489, ss1917990139, ss1958234494, ss1966671079, ss2019511229, ss2147501564, ss2321716112, ss2624271452, ss2697395471, ss2731054482, ss2746194368, ss2750954454, ss2986198749, ss3021047390, ss3343288065, ss3637733669, ss3646220098, ss3651370036, ss3654299820, ss3726738590, ss3745753095, ss3783308410, ss3788985321, ss3793857949, ss3823550230, ss3825551130, ss3825993226, ss3836383723, ss3848065857, ss3892926825, ss3983912913, ss3983912914, ss3984774868, ss3986008141, ss3986095080, ss4016890026, ss5142194374 NC_000001.10:3548135:T:C NC_000001.11:3631571:T:C (self)
820590, 2593, 67072, 2125, 534677, 860267, 6446195544, ss2159561008, ss3023519243, ss3067087364, ss3646586412, ss3686043985, ss3724990704, ss3770780656, ss3798774823, ss3841787872, ss3943689071, ss4437253932, ss5236863339, ss5237158755 NC_000001.11:3631571:T:C NC_000001.11:3631571:T:C (self)
ss12992682, ss16429457, ss20484820 NT_004321.15:854910:T:C NC_000001.11:3631571:T:C (self)
ss3897985, ss4321013, ss6232547, ss6396663, ss16253056, ss23157527, ss67271802, ss67672566, ss68211610, ss70750269, ss71322591, ss75862628, ss84078467, ss86238958, ss97915363, ss105114661, ss139864187, ss154232615, ss154558772, ss159409081, ss159695833, ss173454819 NT_004350.19:3026767:T:C NC_000001.11:3631571: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 rs2760321

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.post596+ae089ad