rs1920773 - SNP

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Select item 19207731.

rs1920773 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 12:91052319 (GRCh38)
12:91446096 (GRCh37)
Canonical SPDI:: NC_000012.12:91052318:T:A,NC_000012.12:91052318:T:G
Gene:: KERA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.121175/2289 (ALFA)
T=0.05/2 (GENOME_DK)
T=0.053571/3 (Siberian)
T=0.072993/40 (SGDP_PRJ)
T=0.073333/44 (NorthernSweden)
T=0.082136/1377 (TOMMO)
T=0.085383/250 (KOREAN)
T=0.095524/175 (Korea1K)
T=0.101562/455 (Estonian)
T=0.101968/511 (1000Genomes)
T=0.105605/407 (ALSPAC)
T=0.105717/392 (TWINSUK)
T=0.112224/112 (GoNL)
T=0.130047/18115 (GnomAD)
T=0.130841/28 (Vietnamese)
T=0.131433/34789 (TOPMED)
T=0.131902/43 (HapMap)
T=0.143519/31 (Qatari)
HGVS:: NC_000012.12:g.91052319T>A, NC_000012.12:g.91052319T>G, NC_000012.11:g.91446096T>A, NC_000012.11:g.91446096T>G, NG_021223.1:g.11036A>T, NG_021223.1:g.11036A>C

Select item 590089572.

rs59008957 has merged into rs1920773 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 12:91052319 (GRCh38)
12:91446096 (GRCh37)
Canonical SPDI:: NC_000012.12:91052318:T:A,NC_000012.12:91052318:T:G
Gene:: KERA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.121175/2289 (ALFA)
T=0.05/2 (GENOME_DK)
T=0.053571/3 (Siberian)
T=0.072993/40 (SGDP_PRJ)
T=0.073333/44 (NorthernSweden)
T=0.082136/1377 (TOMMO)
T=0.085383/250 (KOREAN)
T=0.095524/175 (Korea1K)
T=0.101562/455 (Estonian)
T=0.101968/511 (1000Genomes)
T=0.105605/407 (ALSPAC)
T=0.105717/392 (TWINSUK)
T=0.112224/112 (GoNL)
T=0.130047/18115 (GnomAD)
T=0.130841/28 (Vietnamese)
T=0.131433/34789 (TOPMED)
T=0.131902/43 (HapMap)
T=0.143519/31 (Qatari)
HGVS:: NC_000012.12:g.91052319T>A, NC_000012.12:g.91052319T>G, NC_000012.11:g.91446096T>A, NC_000012.11:g.91446096T>G, NG_021223.1:g.11036A>T, NG_021223.1:g.11036A>C