{{Rsnum
|rsid=137853286
|Chromosome=13
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=ATP7B
|position=51942398
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=13
|CLNALLE=1
|CLNDBN=Wilson's disease
|CLNDSDB=OMIM
|CLNDSDBID=277900
|CLNHGVS=NC_000013.10:g.52516534delG
|CLNSIG=5
|Disease=Wilson's disease
|FwdREF=C
|GENEINFO=ATP7B:540
|GENE_ID=540
|GENE_NAME=ATP7B
|REF=CG
|RSPOS=52516531
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;S3D;NSF;REF;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050268001201000002110200
|WGT=1
|dbSNPBuildID=133
|rsid=137853286
}}{{PMID Auto
|PMID=11857545
|Title=Common mutations of ATP7B in Wilson disease patients from Hungary.
}}

{{PMID Auto
|PMID=12955875
|Title=Diagnosis and phenotypic classification of Wilson disease.
}}

{{PMID Auto
|PMID=16791614
|Title=Regional distribution of mutations of the ATP7B gene in patients with Wilson disease: impact on genetic testing.
}}