rs2421853 - SNP

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Select item 24218531.

rs2421853 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:171630813 (GRCh38)
1:171599953 (GRCh37)
Canonical SPDI:: NC_000001.11:171630812:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.258743/51166 (ALFA)
A=0.151515/10 (PRJEB36033)
A=0.184527/3093 (TOMMO)
A=0.188333/113 (NorthernSweden)
A=0.191139/151 (PRJEB37584)
A=0.196507/360 (Korea1K)
A=0.198294/581 (KOREAN)
A=0.231481/50 (Vietnamese)
A=0.244162/941 (ALSPAC)
A=0.245685/911 (TWINSUK)
A=0.246493/246 (GoNL)
A=0.272321/1220 (Estonian)
A=0.284549/593 (HGDP_Stanford)
A=0.3/12 (GENOME_DK)
A=0.324074/70 (Qatari)
A=0.333441/46639 (GnomAD)
A=0.333605/88302 (TOPMED)
A=0.359151/1799 (1000Genomes)
A=0.370899/701 (HapMap)
G=0.403226/100 (SGDP_PRJ)
G=0.5/14 (Siberian)
HGVS:: NC_000001.11:g.171630813G>A, NC_000001.10:g.171599953G>A

Select item 604845842.

rs60484584 has merged into rs2421853 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:171630813 (GRCh38)
1:171599953 (GRCh37)
Canonical SPDI:: NC_000001.11:171630812:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.258743/51166 (ALFA)
A=0.151515/10 (PRJEB36033)
A=0.184527/3093 (TOMMO)
A=0.188333/113 (NorthernSweden)
A=0.191139/151 (PRJEB37584)
A=0.196507/360 (Korea1K)
A=0.198294/581 (KOREAN)
A=0.231481/50 (Vietnamese)
A=0.244162/941 (ALSPAC)
A=0.245685/911 (TWINSUK)
A=0.246493/246 (GoNL)
A=0.272321/1220 (Estonian)
A=0.284549/593 (HGDP_Stanford)
A=0.3/12 (GENOME_DK)
A=0.324074/70 (Qatari)
A=0.333441/46639 (GnomAD)
A=0.333605/88302 (TOPMED)
A=0.359151/1799 (1000Genomes)
A=0.370899/701 (HapMap)
G=0.403226/100 (SGDP_PRJ)
G=0.5/14 (Siberian)
HGVS:: NC_000001.11:g.171630813G>A, NC_000001.10:g.171599953G>A