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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.

rs56307380

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr6:30164668 (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>G
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.121603 (32187/264690, TOPMED)
A=0.132353 (18545/140118, GnomAD)
A=0.12335 (9699/78632, PAGE_STUDY) (+ 17 more)
A=0.35855 (10132/28258, 14KJPN)
A=0.13750 (2719/19774, ALFA)
A=0.35996 (6033/16760, 8.3KJPN)
A=0.1686 (1080/6404, 1000G_30x)
A=0.1739 (871/5008, 1000G)
A=0.1710 (766/4480, Estonian)
A=0.1541 (594/3854, ALSPAC)
A=0.1605 (595/3708, TWINSUK)
A=0.2737 (802/2930, KOREAN)
A=0.163 (163/998, GoNL)
A=0.205 (123/600, NorthernSweden)
A=0.116 (25/216, Qatari)
C=0.401 (85/212, SGDP_PRJ)
A=0.410 (87/212, Vietnamese)
A=0.24 (22/92, Ancient Sardinia)
A=0.12 (5/40, GENOME_DK)
C=0.46 (12/26, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TRIM15 : Intron Variant
TRIM10 : 2KB Upstream 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 19774 C=0.86250 A=0.13750
European Sub 14370 C=0.83841 A=0.16159
African Sub 3400 C=0.9559 A=0.0441
African Others Sub 114 C=0.991 A=0.009
African American Sub 3286 C=0.9547 A=0.0453
Asian Sub 118 C=0.729 A=0.271
East Asian Sub 90 C=0.74 A=0.26
Other Asian Sub 28 C=0.68 A=0.32
Latin American 1 Sub 154 C=0.896 A=0.104
Latin American 2 Sub 616 C=0.886 A=0.114
South Asian Sub 100 C=0.82 A=0.18
Other Sub 1016 C=0.8907 A=0.1093


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 C=0.878397 A=0.121603
gnomAD - Genomes Global Study-wide 140118 C=0.867647 A=0.132353
gnomAD - Genomes European Sub 75848 C=0.82130 A=0.17870
gnomAD - Genomes African Sub 42022 C=0.95993 A=0.04007
gnomAD - Genomes American Sub 13652 C=0.88126 A=0.11874
gnomAD - Genomes Ashkenazi Jewish Sub 3318 C=0.8659 A=0.1341
gnomAD - Genomes East Asian Sub 3128 C=0.6998 A=0.3002
gnomAD - Genomes Other Sub 2150 C=0.8595 A=0.1405
The PAGE Study Global Study-wide 78632 C=0.87665 A=0.12335
The PAGE Study AfricanAmerican Sub 32490 C=0.95494 A=0.04506
The PAGE Study Mexican Sub 10794 C=0.89040 A=0.10960
The PAGE Study Asian Sub 8308 C=0.6476 A=0.3524
The PAGE Study PuertoRican Sub 7910 C=0.9032 A=0.0968
The PAGE Study NativeHawaiian Sub 4532 C=0.6573 A=0.3427
The PAGE Study Cuban Sub 4228 C=0.8588 A=0.1412
The PAGE Study Dominican Sub 3828 C=0.9046 A=0.0954
The PAGE Study CentralAmerican Sub 2448 C=0.9007 A=0.0993
The PAGE Study SouthAmerican Sub 1978 C=0.8862 A=0.1138
The PAGE Study NativeAmerican Sub 1260 C=0.8571 A=0.1429
The PAGE Study SouthAsian Sub 856 C=0.772 A=0.228
14KJPN JAPANESE Study-wide 28258 C=0.64145 A=0.35855
Allele Frequency Aggregator Total Global 19774 C=0.86250 A=0.13750
Allele Frequency Aggregator European Sub 14370 C=0.83841 A=0.16159
Allele Frequency Aggregator African Sub 3400 C=0.9559 A=0.0441
Allele Frequency Aggregator Other Sub 1016 C=0.8907 A=0.1093
Allele Frequency Aggregator Latin American 2 Sub 616 C=0.886 A=0.114
Allele Frequency Aggregator Latin American 1 Sub 154 C=0.896 A=0.104
Allele Frequency Aggregator Asian Sub 118 C=0.729 A=0.271
Allele Frequency Aggregator South Asian Sub 100 C=0.82 A=0.18
8.3KJPN JAPANESE Study-wide 16760 C=0.64004 A=0.35996
1000Genomes_30x Global Study-wide 6404 C=0.8314 A=0.1686
1000Genomes_30x African Sub 1786 C=0.9888 A=0.0112
1000Genomes_30x Europe Sub 1266 C=0.8183 A=0.1817
1000Genomes_30x South Asian Sub 1202 C=0.7496 A=0.2504
1000Genomes_30x East Asian Sub 1170 C=0.6402 A=0.3598
1000Genomes_30x American Sub 980 C=0.890 A=0.110
1000Genomes Global Study-wide 5008 C=0.8261 A=0.1739
1000Genomes African Sub 1322 C=0.9864 A=0.0136
1000Genomes East Asian Sub 1008 C=0.6429 A=0.3571
1000Genomes Europe Sub 1006 C=0.8191 A=0.1809
1000Genomes South Asian Sub 978 C=0.755 A=0.245
1000Genomes American Sub 694 C=0.898 A=0.102
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.8290 A=0.1710
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.8459 A=0.1541
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.8395 A=0.1605
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.7263 A=0.2737, G=0.0000
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.837 A=0.163
Northern Sweden ACPOP Study-wide 600 C=0.795 A=0.205
Qatari Global Study-wide 216 C=0.884 A=0.116
SGDP_PRJ Global Study-wide 212 C=0.401 A=0.599
A Vietnamese Genetic Variation Database Global Study-wide 212 C=0.590 A=0.410
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 92 C=0.76 A=0.24
The Danish reference pan genome Danish Study-wide 40 C=0.88 A=0.12
Siberian Global Study-wide 26 C=0.46 A=0.54
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 6 NC_000006.12:g.30164668C>A
GRCh38.p14 chr 6 NC_000006.12:g.30164668C>G
GRCh37.p13 chr 6 NC_000006.11:g.30132445C>A
GRCh37.p13 chr 6 NC_000006.11:g.30132445C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.1644466C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.1644466C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.1644572C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.1644572C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.1419796C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.1419796C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.1425392C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.1425392C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.1420569C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.1420569C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.1426154C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.1426154C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.1463599C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.1463599C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.1462897C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.1462897C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.1475370C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.1475370C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.1480990C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.1480990C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.1508741C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.1508741C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.1514326C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.1514326C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.1422748C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.1422748C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.1372664C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.1372664C>G
Gene: TRIM15, tripartite motif containing 15 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TRIM15 transcript NM_033229.3:c.381+603C>A N/A Intron Variant
TRIM15 transcript variant X1 XM_011514987.2:c.66+603C>A N/A Intron Variant
TRIM15 transcript variant X3 XM_047419503.1:c.381+603C…

XM_047419503.1:c.381+603C>A

 		N/A Intron Variant
TRIM15 transcript variant X2 XM_011514988.3:c. N/A Genic Upstream Transcript Variant
Gene: TRIM10, tripartite motif containing 10 (minus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
TRIM10 transcript variant 1 NM_006778.4:c. N/A N/A
TRIM10 transcript variant 2 NM_052828.3:c. N/A N/A
TRIM10 transcript variant X4 XM_011514221.2:c. N/A Upstream Transcript Variant
TRIM10 transcript variant X1 XM_011514222.3:c. N/A Upstream Transcript Variant
TRIM10 transcript variant X2 XM_011514223.3:c. N/A Upstream Transcript Variant
TRIM10 transcript variant X5 XM_047418051.1:c. N/A Upstream Transcript Variant
TRIM10 transcript variant X6 XM_047418052.1:c. N/A Upstream Transcript Variant
TRIM10 transcript variant X3 XM_047418053.1:c. N/A Upstream 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 C= A G
GRCh38.p14 chr 6 NC_000006.12:g.30164668= NC_000006.12:g.30164668C>A NC_000006.12:g.30164668C>G
GRCh37.p13 chr 6 NC_000006.11:g.30132445= NC_000006.11:g.30132445C>A NC_000006.11:g.30132445C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.1644466= NT_113891.3:g.1644466C>A NT_113891.3:g.1644466C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.1644572= NT_113891.2:g.1644572C>A NT_113891.2:g.1644572C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.1419796= NT_167248.2:g.1419796C>A NT_167248.2:g.1419796C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.1425392= NT_167248.1:g.1425392C>A NT_167248.1:g.1425392C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.1420569= NT_167245.2:g.1420569C>A NT_167245.2:g.1420569C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.1426154= NT_167245.1:g.1426154C>A NT_167245.1:g.1426154C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.1463599= NT_167249.2:g.1463599C>A NT_167249.2:g.1463599C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.1462897= NT_167249.1:g.1462897C>A NT_167249.1:g.1462897C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.1475370= NT_167246.2:g.1475370C>A NT_167246.2:g.1475370C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.1480990= NT_167246.1:g.1480990C>A NT_167246.1:g.1480990C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.1508741= NT_167247.2:g.1508741C>A NT_167247.2:g.1508741C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.1514326= NT_167247.1:g.1514326C>A NT_167247.1:g.1514326C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.1422748= NT_167244.2:g.1422748C>A NT_167244.2:g.1422748C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.1372664= NT_167244.1:g.1372664C>A NT_167244.1:g.1372664C>G
TRIM15 transcript NM_033229.2:c.381+603= NM_033229.2:c.381+603C>A NM_033229.2:c.381+603C>G
TRIM15 transcript NM_033229.3:c.381+603= NM_033229.3:c.381+603C>A NM_033229.3:c.381+603C>G
TRIM15 transcript variant X1 XM_005249471.1:c.381+603= XM_005249471.1:c.381+603C>A XM_005249471.1:c.381+603C>G
TRIM15 transcript variant X1 XM_005272907.1:c.381+603= XM_005272907.1:c.381+603C>A XM_005272907.1:c.381+603C>G
TRIM15 transcript variant X1 XM_005274898.1:c.381+603= XM_005274898.1:c.381+603C>A XM_005274898.1:c.381+603C>G
TRIM15 transcript variant X1 XM_005275063.1:c.381+603= XM_005275063.1:c.381+603C>A XM_005275063.1:c.381+603C>G
TRIM15 transcript variant X1 XM_005275195.1:c.381+603= XM_005275195.1:c.381+603C>A XM_005275195.1:c.381+603C>G
TRIM15 transcript variant X1 XM_005275319.1:c.381+603= XM_005275319.1:c.381+603C>A XM_005275319.1:c.381+603C>G
TRIM15 transcript variant X1 XM_005275490.1:c.381+603= XM_005275490.1:c.381+603C>A XM_005275490.1:c.381+603C>G
TRIM15 transcript variant X1 XM_005275628.1:c.381+603= XM_005275628.1:c.381+603C>A XM_005275628.1:c.381+603C>G
TRIM15 transcript variant X1 XM_011514987.2:c.66+603= XM_011514987.2:c.66+603C>A XM_011514987.2:c.66+603C>G
TRIM15 transcript variant X3 XM_047419503.1:c.381+603= XM_047419503.1:c.381+603C>A XM_047419503.1:c.381+603C>G
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#.

67 SubSNP, 20 Frequency submissions
No Submitter Submission ID Date (Build)
1 HGSV ss77798091 Dec 07, 2007 (129)
2 BCMHGSC_JDW ss93432742 Mar 24, 2008 (130)
3 BGI ss104293563 Dec 01, 2009 (131)
4 1000GENOMES ss109880043 Feb 13, 2009 (137)
5 GMI ss156708166 Dec 01, 2009 (131)
6 1000GENOMES ss233387176 Jul 14, 2010 (137)
7 1000GENOMES ss240458911 Jul 15, 2010 (137)
8 GMI ss278714450 May 04, 2012 (137)
9 GMI ss285368797 Apr 25, 2013 (138)
10 ILLUMINA ss535690295 Sep 08, 2015 (146)
11 TISHKOFF ss559101836 Apr 25, 2013 (138)
12 SSMP ss653018997 Apr 25, 2013 (138)
13 EVA-GONL ss982744500 Aug 21, 2014 (142)
14 JMKIDD_LAB ss1073492759 Aug 21, 2014 (142)
15 1000GENOMES ss1319512487 Aug 21, 2014 (142)
16 EVA_GENOME_DK ss1581596320 Apr 01, 2015 (144)
17 EVA_DECODE ss1592291873 Apr 01, 2015 (144)
18 EVA_UK10K_ALSPAC ss1615251150 Apr 01, 2015 (144)
19 EVA_UK10K_TWINSUK ss1658245183 Apr 01, 2015 (144)
20 WEILL_CORNELL_DGM ss1925996681 Feb 12, 2016 (147)
21 ILLUMINA ss1958881432 Feb 12, 2016 (147)
22 JJLAB ss2023626737 Sep 14, 2016 (149)
23 ILLUMINA ss2094952445 Dec 20, 2016 (150)
24 ILLUMINA ss2095174703 Dec 20, 2016 (150)
25 USC_VALOUEV ss2151792024 Nov 08, 2017 (151)
26 HUMAN_LONGEVITY ss2282872983 Dec 20, 2016 (150)
27 SYSTEMSBIOZJU ss2626299434 Nov 08, 2017 (151)
28 GRF ss2707384090 Nov 08, 2017 (151)
29 GNOMAD ss2837313601 Nov 08, 2017 (151)
30 SWEGEN ss2998765673 Nov 08, 2017 (151)
31 ILLUMINA ss3022593136 Nov 08, 2017 (151)
32 BIOINF_KMB_FNS_UNIBA ss3025598517 Nov 08, 2017 (151)
33 ILLUMINA ss3629492531 Oct 12, 2018 (152)
34 ILLUMINA ss3653104160 Oct 12, 2018 (152)
35 EGCUT_WGS ss3666688123 Jul 13, 2019 (153)
36 EVA_DECODE ss3716876066 Jul 13, 2019 (153)
37 ILLUMINA ss3726325703 Jul 13, 2019 (153)
38 ACPOP ss3733340524 Jul 13, 2019 (153)
39 EVA ss3764799242 Jul 13, 2019 (153)
40 PAGE_CC ss3771275101 Jul 13, 2019 (153)
41 KHV_HUMAN_GENOMES ss3807954798 Jul 13, 2019 (153)
42 EVA ss3829817426 Apr 26, 2020 (154)
43 EVA ss3838385901 Apr 26, 2020 (154)
44 EVA ss3843827224 Apr 26, 2020 (154)
45 SGDP_PRJ ss3864220315 Apr 26, 2020 (154)
46 KRGDB ss3910994981 Apr 26, 2020 (154)
47 EVA ss3985210533 Apr 26, 2021 (155)
48 VINODS ss4025169883 Apr 26, 2021 (155)
49 VINODS ss4025222612 Apr 26, 2021 (155)
50 VINODS ss4025242667 Apr 26, 2021 (155)
51 TOPMED ss4698103046 Apr 26, 2021 (155)
52 TOMMO_GENOMICS ss5176782026 Apr 26, 2021 (155)
53 EVA ss5237392655 Apr 26, 2021 (155)
54 1000G_HIGH_COVERAGE ss5267893293 Oct 13, 2022 (156)
55 EVA ss5364661075 Oct 13, 2022 (156)
56 HUGCELL_USP ss5465634655 Oct 13, 2022 (156)
57 1000G_HIGH_COVERAGE ss5553537195 Oct 13, 2022 (156)
58 SANFORD_IMAGENETICS ss5624620860 Oct 13, 2022 (156)
59 SANFORD_IMAGENETICS ss5640057980 Oct 13, 2022 (156)
60 TOMMO_GENOMICS ss5714621484 Oct 13, 2022 (156)
61 YY_MCH ss5807285713 Oct 13, 2022 (156)
62 EVA ss5842000568 Oct 13, 2022 (156)
63 EVA ss5847288532 Oct 13, 2022 (156)
64 EVA ss5855271274 Oct 13, 2022 (156)
65 EVA ss5883200420 Oct 13, 2022 (156)
66 EVA ss5968561357 Oct 13, 2022 (156)
67 EVA ss5979776942 Oct 13, 2022 (156)
68 1000Genomes NC_000006.11 - 30132445 Oct 12, 2018 (152)
69 1000Genomes_30x NC_000006.12 - 30164668 Oct 13, 2022 (156)
70 The Avon Longitudinal Study of Parents and Children NC_000006.11 - 30132445 Oct 12, 2018 (152)
71 Genetic variation in the Estonian population NC_000006.11 - 30132445 Oct 12, 2018 (152)
72 The Danish reference pan genome NC_000006.11 - 30132445 Apr 26, 2020 (154)
73 gnomAD - Genomes NC_000006.12 - 30164668 Apr 26, 2021 (155)
74 Genome of the Netherlands Release 5 NC_000006.11 - 30132445 Apr 26, 2020 (154)
75 KOREAN population from KRGDB NC_000006.11 - 30132445 Apr 26, 2020 (154)
76 Northern Sweden NC_000006.11 - 30132445 Jul 13, 2019 (153)
77 The PAGE Study NC_000006.12 - 30164668 Jul 13, 2019 (153)
78 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000006.11 - 30132445 Apr 26, 2021 (155)
79 Qatari NC_000006.11 - 30132445 Apr 26, 2020 (154)
80 SGDP_PRJ NC_000006.11 - 30132445 Apr 26, 2020 (154)
81 Siberian NC_000006.11 - 30132445 Apr 26, 2020 (154)
82 8.3KJPN NC_000006.11 - 30132445 Apr 26, 2021 (155)
83 14KJPN NC_000006.12 - 30164668 Oct 13, 2022 (156)
84 TopMed NC_000006.12 - 30164668 Apr 26, 2021 (155)
85 UK 10K study - Twins NC_000006.11 - 30132445 Oct 12, 2018 (152)
86 A Vietnamese Genetic Variation Database NC_000006.11 - 30132445 Jul 13, 2019 (153)
87 ALFA NC_000006.12 - 30164668 Apr 26, 2021 (155)
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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)
rs62407494 May 23, 2008 (130)
rs114562747 May 04, 2012 (137)
rs117237425 Aug 16, 2010 (132)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss77798091 NC_000006.9:30240423:C:A NC_000006.12:30164667:C:A (self)
ss93432742, ss109880043, ss278714450, ss285368797, ss1592291873, ss2094952445 NC_000006.10:30240423:C:A NC_000006.12:30164667:C:A (self)
31277905, 17437595, 12426371, 7761259, 7744559, 18172375, 6625389, 436460, 8038611, 16237295, 4308378, 34751333, 17437595, 3863300, ss233387176, ss240458911, ss535690295, ss559101836, ss653018997, ss982744500, ss1073492759, ss1319512487, ss1581596320, ss1615251150, ss1658245183, ss1925996681, ss1958881432, ss2023626737, ss2095174703, ss2151792024, ss2626299434, ss2707384090, ss2837313601, ss2998765673, ss3022593136, ss3629492531, ss3653104160, ss3666688123, ss3733340524, ss3764799242, ss3829817426, ss3838385901, ss3864220315, ss3910994981, ss3985210533, ss5176782026, ss5237392655, ss5364661075, ss5624620860, ss5640057980, ss5842000568, ss5847288532, ss5968561357, ss5979776942 NC_000006.11:30132444:C:A NC_000006.12:30164667:C:A (self)
41063130, 220951114, 496570, 48458588, 535480604, 10102069124, ss2282872983, ss3025598517, ss3716876066, ss3726325703, ss3771275101, ss3807954798, ss3843827224, ss4698103046, ss5267893293, ss5465634655, ss5553537195, ss5714621484, ss5807285713, ss5855271274, ss5883200420 NC_000006.12:30164667:C:A NC_000006.12:30164667:C:A (self)
ss104293563, ss156708166 NT_007592.15:30072444:C:A NC_000006.12:30164667:C:A (self)
ss4025169883 NT_167244.2:1422747:C:A NC_000006.12:30164667:C:A (self)
ss4025222612 NT_167246.2:1475369:C:A NC_000006.12:30164667:C:A (self)
ss4025242667 NT_167247.2:1508740:C:A NC_000006.12:30164667:C:A (self)
18172375, ss3910994981 NC_000006.11:30132444:C:G NC_000006.12:30164667:C:G (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs56307380

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.post774+babeb33