{{Rsnum
|rsid=11554495
|Gene=KRT8
|Chromosome=12
|position=52904798
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|GMAF=0.002755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=KRT8
}}{{omim
|desc=CIRRHOSIS, CRYPTOGENIC
|id=148060
|rsnum=11554495
|variant=0001
}}

{{ClinVar
|rsid=11554495
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=53298582
|CHROM=12
|GMAF=0.0027
|dbSNPBuildID=120
|SSR=0
|SAO=1
|VP=0x050160000000040116110100
|GENEINFO=KRT8:3856
|GENE_NAME=KRT8
|GENE_ID=3856
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.53298582C>A
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;SLO;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9972; 0.002755
|CLNACC=RCV000015735.24; RCV000015736.1; RCV000056938.1
|CLNDBN=Cirrhosis, cryptogenic; Cirrhosis, noncryptogenic, susceptibility to; not provided
|CLNDSDB=MedGen
|CLNDSDBID=C0267809; C1835713
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNSRCID=KRT8:c.184G>T; 148060.0001
|COMMON=1
|Disease=Cirrhosis; not provided
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}