{{Rsnum
|rsid=193922110
|Chromosome=13
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ATP7B
|position=51935659
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922110
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=52509795
|CHROM=13
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000013.10:g.52509795C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Wilson's disease
|Disease=Wilson's disease
|Tags=RV;PM;PMC;OTHERKG;LSD
|CLNACC=RCV000029378.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1512:C0019202:277900:905:88518009
|GENEINFO=ATP7B:540
|GENE_ID=540
|GENE_NAME=ATP7B
}}{{PMID Auto
|PMID=10502777
|Title=A study of Wilson disease mutations in Britain.
}}