rs1920726 - SNP

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Select item 19207261.

rs1920726 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 12:91078587 (GRCh38)
12:91472364 (GRCh37)
Canonical SPDI:: NC_000012.12:91078586:T:A,NC_000012.12:91078586:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.034587/1067 (ALFA)
T=0./0 (GENOME_DK)
T=0./0 (Korea1K)
T=0./0 (TOMMO)
T=0./0 (Vietnamese)
T=0.001024/3 (KOREAN)
T=0.009025/5 (SGDP_PRJ)
T=0.017857/1 (Siberian)
T=0.018333/11 (NorthernSweden)
T=0.02436/122 (1000Genomes)
T=0.02439/8 (HapMap)
T=0.029839/115 (ALSPAC)
T=0.032366/145 (Estonian)
T=0.033441/124 (TWINSUK)
T=0.035865/9493 (TOPMED)
T=0.036512/5113 (GnomAD)
T=0.039078/39 (GoNL)
T=0.050926/11 (Qatari)
HGVS:: NC_000012.12:g.91078587T>A, NC_000012.12:g.91078587T>C, NC_000012.11:g.91472364T>A, NC_000012.11:g.91472364T>C

Select item 607424742.

rs60742474 has merged into rs1920726 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 12:91078587 (GRCh38)
12:91472364 (GRCh37)
Canonical SPDI:: NC_000012.12:91078586:T:A,NC_000012.12:91078586:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.034587/1067 (ALFA)
T=0./0 (GENOME_DK)
T=0./0 (Korea1K)
T=0./0 (TOMMO)
T=0./0 (Vietnamese)
T=0.001024/3 (KOREAN)
T=0.009025/5 (SGDP_PRJ)
T=0.017857/1 (Siberian)
T=0.018333/11 (NorthernSweden)
T=0.02436/122 (1000Genomes)
T=0.02439/8 (HapMap)
T=0.029839/115 (ALSPAC)
T=0.032366/145 (Estonian)
T=0.033441/124 (TWINSUK)
T=0.035865/9493 (TOPMED)
T=0.036512/5113 (GnomAD)
T=0.039078/39 (GoNL)
T=0.050926/11 (Qatari)
HGVS:: NC_000012.12:g.91078587T>A, NC_000012.12:g.91078587T>C, NC_000012.11:g.91472364T>A, NC_000012.11:g.91472364T>C