{{Rsnum
|rsid=57749775
|Gene=KRT8
|Chromosome=12
|position=52904822
|Orientation=plus
|GMAF=0.002755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=KRT8
}}{{omim
|id=148060
|rsnum=57749775
|variant=0002
}}

{{ClinVar
|rsid=57749775
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=53298606
|CHROM=12
|GMAF=0.0027
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x05016000000004011e110100
|GENEINFO=KRT8:3856
|GENE_NAME=KRT8
|GENE_ID=3856
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.53298606A>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;SLO;VLD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;LSD;OM
|CAF=0.9972; 0.002755
|CLNACC=RCV000015737.24; RCV000056936.1
|CLNDBN=Cirrhosis, cryptogenic; not provided
|CLNDSDB=MedGen
|CLNDSDBID=C0267809
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNSRCID=KRT8:c.160T>C; 148060.0002
|COMMON=1
|Disease=Cirrhosis; not provided
}}

{{GET Evidence
|gene=KRT8
|aa_change=Tyr54His
|aa_change_short=Y54H
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs57749775
|overall_frequency_n=58
|overall_frequency_d=10608
|overall_frequency=0.00546757
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.56
|nblosum100=-1
|autoscore=1
|webscore=N
}}

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