rs6721964 - SNP

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Select item 67219641.

rs6721964 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 2:190713628 (GRCh38)
2:191578354 (GRCh37)
Canonical SPDI:: NC_000002.12:190713627:G:A,NC_000002.12:190713627:G:C
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.338268/82256 (ALFA)
G=0.25/10 (GENOME_DK)
G=0.272727/12 (Siberian)
G=0.282407/61 (Qatari)
G=0.292035/132 (SGDP_PRJ)
G=0.319921/44796 (GnomAD)
G=0.322006/1194 (TWINSUK)
G=0.327889/86789 (TOPMED)
G=0.332641/1282 (ALSPAC)
G=0.350534/27587 (PAGE_STUDY)
G=0.350633/277 (PRJEB37584)
G=0.352705/352 (GoNL)
G=0.375/114 (HapMap)
G=0.377902/1693 (Estonian)
G=0.380205/1114 (KOREAN)
G=0.381667/229 (NorthernSweden)
G=0.401156/2009 (1000Genomes)
G=0.435412/7298 (TOMMO)
A=0.449074/97 (Vietnamese)
HGVS:: NC_000002.12:g.190713628G>A, NC_000002.12:g.190713628G>C, NC_000002.11:g.191578354G>A, NC_000002.11:g.191578354G>C

Select item 594999302.

rs59499930 has merged into rs6721964 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 2:190713628 (GRCh38)
2:191578354 (GRCh37)
Canonical SPDI:: NC_000002.12:190713627:G:A,NC_000002.12:190713627:G:C
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.338268/82256 (ALFA)
G=0.25/10 (GENOME_DK)
G=0.272727/12 (Siberian)
G=0.282407/61 (Qatari)
G=0.292035/132 (SGDP_PRJ)
G=0.319921/44796 (GnomAD)
G=0.322006/1194 (TWINSUK)
G=0.327889/86789 (TOPMED)
G=0.332641/1282 (ALSPAC)
G=0.350534/27587 (PAGE_STUDY)
G=0.350633/277 (PRJEB37584)
G=0.352705/352 (GoNL)
G=0.375/114 (HapMap)
G=0.377902/1693 (Estonian)
G=0.380205/1114 (KOREAN)
G=0.381667/229 (NorthernSweden)
G=0.401156/2009 (1000Genomes)
G=0.435412/7298 (TOMMO)
A=0.449074/97 (Vietnamese)
HGVS:: NC_000002.12:g.190713628G>A, NC_000002.12:g.190713628G>C, NC_000002.11:g.191578354G>A, NC_000002.11:g.191578354G>C