{{Rsnum
|rsid=137853279
|Chromosome=13
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ATP7B
|position=51941111
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=606882
|variant=0021
|rsnum=137853279
}}{{ClinVar
|rsid=137853279
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=52515247
|CHROM=13
|dbSNPBuildID=133
|SSR=0
|SAO=0
|VP=0x050268000000000002110100
|GENEINFO=ATP7B:540
|GENE_NAME=ATP7B
|GENE_ID=540
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000013.10:g.52515247C>T
|CLNSRCID=
606882.0021
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000004067.1
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDBN=Wilson's disease
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1512:C0019202:277900:905:88518009
|CLNSRC=OMIM Allelic Variant
|Disease=Wilson's disease
}}{{PMID Auto
|PMID=9887381
|Title=His1069Gln and six novel Wilson disease mutations: analysis of relevance for early diagnosis and phenotype.
}}

{{PMID Auto
|PMID=15845031
|Title=Wilson disease: high prevalence in a mountainous area of Crete.
}}