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Select item 19207751.

rs1920775 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 12:91055297 (GRCh38)
12:91449074 (GRCh37)
Canonical SPDI:: NC_000012.12:91055296:G:A,NC_000012.12:91055296:G:T
Gene:: KERA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.054344/7774 (ALFA)
A=0./0 (PRJEB36033)
A=0.001092/2 (Korea1K)
A=0.001451/24 (TOMMO)
A=0.001711/5 (KOREAN)
A=0.025/15 (NorthernSweden)
A=0.041199/22 (MGP)
A=0.041787/87 (HGDP_Stanford)
A=0.046705/180 (ALSPAC)
A=0.049083/182 (TWINSUK)
A=0.055556/12 (Qatari)
A=0.064959/325 (1000Genomes)
A=0.067857/304 (Estonian)
A=0.068136/68 (GoNL)
A=0.069106/119 (HapMap)
A=0.07153/9953 (GnomAD)
A=0.074234/19649 (TOPMED)
A=0.15/6 (GENOME_DK)
G=0.5/1 (Siberian)
G=0.5/20 (SGDP_PRJ)
HGVS:: NC_000012.12:g.91055297G>A, NC_000012.12:g.91055297G>T, NC_000012.11:g.91449074G>A, NC_000012.11:g.91449074G>T, NG_021223.1:g.8058C>T, NG_021223.1:g.8058C>A

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