rs734722 - SNP

Select item 7347221.

rs734722 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:91055135 (GRCh38)
12:91448912 (GRCh37)
Canonical SPDI:: NC_000012.12:91055134:C:T
Gene:: KERA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.203611/32941 (ALFA)
T=0.125/4 (PRJEB36033)
T=0.163333/98 (NorthernSweden)
T=0.174488/647 (TWINSUK)
T=0.176959/682 (ALSPAC)
T=0.191071/856 (Estonian)
T=0.192385/192 (GoNL)
T=0.209174/3506 (TOMMO)
T=0.225/9 (GENOME_DK)
T=0.235495/690 (KOREAN)
T=0.235849/50 (Vietnamese)
T=0.251638/461 (Korea1K)
T=0.263889/57 (Qatari)
T=0.294146/613 (HGDP_Stanford)
T=0.325168/45184 (GnomAD)
T=0.343662/90964 (TOPMED)
C=0.359375/92 (SGDP_PRJ)
T=0.367427/1840 (1000Genomes)
T=0.399049/755 (HapMap)
C=0.5/8 (Siberian)
HGVS:: NC_000012.12:g.91055135C>T, NC_000012.11:g.91448912C>T, NG_021223.1:g.8220G>A

Select item 3866094602.

rs386609460 has merged into rs734722 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:91055135 (GRCh38)
12:91448912 (GRCh37)
Canonical SPDI:: NC_000012.12:91055134:C:T
Gene:: KERA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.203611/32941 (ALFA)
T=0.125/4 (PRJEB36033)
T=0.163333/98 (NorthernSweden)
T=0.174488/647 (TWINSUK)
T=0.176959/682 (ALSPAC)
T=0.191071/856 (Estonian)
T=0.192385/192 (GoNL)
T=0.209174/3506 (TOMMO)
T=0.225/9 (GENOME_DK)
T=0.235495/690 (KOREAN)
T=0.235849/50 (Vietnamese)
T=0.251638/461 (Korea1K)
T=0.263889/57 (Qatari)
T=0.294146/613 (HGDP_Stanford)
T=0.325168/45184 (GnomAD)
T=0.343662/90964 (TOPMED)
C=0.359375/92 (SGDP_PRJ)
T=0.367427/1840 (1000Genomes)
T=0.399049/755 (HapMap)
C=0.5/8 (Siberian)
HGVS:: NC_000012.12:g.91055135C>T, NC_000012.11:g.91448912C>T, NG_021223.1:g.8220G>A

Select item 616412113.

rs61641211 has merged into rs734722 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:91055135 (GRCh38)
12:91448912 (GRCh37)
Canonical SPDI:: NC_000012.12:91055134:C:T
Gene:: KERA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.203611/32941 (ALFA)
T=0.125/4 (PRJEB36033)
T=0.163333/98 (NorthernSweden)
T=0.174488/647 (TWINSUK)
T=0.176959/682 (ALSPAC)
T=0.191071/856 (Estonian)
T=0.192385/192 (GoNL)
T=0.209174/3506 (TOMMO)
T=0.225/9 (GENOME_DK)
T=0.235495/690 (KOREAN)
T=0.235849/50 (Vietnamese)
T=0.251638/461 (Korea1K)
T=0.263889/57 (Qatari)
T=0.294146/613 (HGDP_Stanford)
T=0.325168/45184 (GnomAD)
T=0.343662/90964 (TOPMED)
C=0.359375/92 (SGDP_PRJ)
T=0.367427/1840 (1000Genomes)
T=0.399049/755 (HapMap)
C=0.5/8 (Siberian)
HGVS:: NC_000012.12:g.91055135C>T, NC_000012.11:g.91448912C>T, NG_021223.1:g.8220G>A

dbSNP