{{Rsnum
|rsid=57758506
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=KRT18
|position=52949556
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KRT8,KRT18
}}{{omim
|id=148070
|rsnum=57758506
|variant=0001
}}{{ClinVar
|rsid=57758506
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=53343340
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000040002110100
|GENEINFO=KRT8:3856; KRT18:3875
|GENE_NAME=KRT8; KRT18
|GENE_ID=3856; 3875
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.53343340A>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;SLO;VLD;OTHERKG;LSD;OM
|CLNACC=RCV000015686.20; RCV000015687.1; RCV000056435.1
|CLNDBN=Cirrhosis, cryptogenic; Cirrhosis, noncryptogenic, susceptibility to; not provided
|CLNDSDB=MedGen
|CLNDSDBID=C0267809; C1835713
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNSRCID=KRT18:c.383A>T; 148070.0001
|Disease=Cirrhosis; not provided
}}