{{Rsnum
|rsid=121909100
|Chromosome=18
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ATP8B1
|position=57669433
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATP8B1,LOC100505549
}}{{omim
|id=602397
|rsnum=121909100
|variant=0006
}}{{ClinVar
|rsid=121909100
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=55336665
|CHROM=18
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040002110100
|GENEINFO=ATP8B1:5205; RP11-35G9.3:100505549
|GENE_NAME=ATP8B1; RP11-35G9.3
|GENE_ID=5205; 100505549
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000018.9:g.55336665A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602397.0006
|CLNSIG=5
|CLNCUI=C1855731; C0268312
|CLNDBN=Benign recurrent intrahepatic cholestasis 1; Progressive intrahepatic cholestasis
|Disease=Benign recurrent intrahepatic cholestasis 1; Progressive intrahepatic cholestasis
|CLNACC=RCV000007689.1; RCV000007690.1
|Tags=RV;PM;S3D;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1297:C1855731:243300:65682; NBK1297:C0268312:211600:172:79306:74162007
}}