rs232610 - SNP

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Select item 2326101.

rs232610 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:38141089 (GRCh38)
2:38368231 (GRCh37)
Canonical SPDI:: NC_000002.12:38141088:A:G
Gene:: CYP1B1-AS1 (Varview), LOC107985871 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.475706/93852 (ALFA)
G=0.107477/23 (Vietnamese)
G=0.112074/1878 (TOMMO)
G=0.134471/394 (KOREAN)
G=0.162118/297 (Korea1K)
A=0.333333/8 (Siberian)
A=0.346939/102 (SGDP_PRJ)
G=0.379079/790 (HGDP_Stanford)
G=0.421611/2111 (1000Genomes)
G=0.428571/6 (PRJEB36033)
G=0.441836/828 (HapMap)
G=0.446667/268 (NorthernSweden)
A=0.45/18 (GENOME_DK)
G=0.453614/1682 (TWINSUK)
G=0.47535/1832 (ALSPAC)
G=0.483947/128096 (TOPMED)
G=0.48998/489 (GoNL)
G=0.492634/2207 (Estonian)
G=0.498672/69843 (GnomAD)
A=0.5/108 (Qatari)
HGVS:: NC_000002.12:g.38141089A>G, NC_000002.11:g.38368231A>G

Select item 579511962.

rs57951196 has merged into rs232610 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:38141089 (GRCh38)
2:38368231 (GRCh37)
Canonical SPDI:: NC_000002.12:38141088:A:G
Gene:: CYP1B1-AS1 (Varview), LOC107985871 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.475706/93852 (ALFA)
G=0.107477/23 (Vietnamese)
G=0.112074/1878 (TOMMO)
G=0.134471/394 (KOREAN)
G=0.162118/297 (Korea1K)
A=0.333333/8 (Siberian)
A=0.346939/102 (SGDP_PRJ)
G=0.379079/790 (HGDP_Stanford)
G=0.421611/2111 (1000Genomes)
G=0.428571/6 (PRJEB36033)
G=0.441836/828 (HapMap)
G=0.446667/268 (NorthernSweden)
A=0.45/18 (GENOME_DK)
G=0.453614/1682 (TWINSUK)
G=0.47535/1832 (ALSPAC)
G=0.483947/128096 (TOPMED)
G=0.48998/489 (GoNL)
G=0.492634/2207 (Estonian)
G=0.498672/69843 (GnomAD)
A=0.5/108 (Qatari)
HGVS:: NC_000002.12:g.38141089A>G, NC_000002.11:g.38368231A>G