{{Rsnum
|rsid=137853285
|Chromosome=13
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ATP7B
|position=51958538
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=13
|CLNALLE=1
|CLNDBN=Wilson's disease
|CLNDSDB=OMIM
|CLNDSDBID=277900
|CLNHGVS=NC_000013.10:g.52532674C>T
|CLNSIG=5
|Disease=Wilson's disease
|FwdALT=A
|FwdREF=G
|GENEINFO=ATP7B:540
|GENE_ID=540
|GENE_NAME=ATP7B
|REF=C
|RSPOS=52532674
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;S3D;NSM;REF;INT;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050268080a01000002110100
|WGT=1
|dbSNPBuildID=133
|rsid=137853285
}}{{PMID Auto
|PMID=11857545
|Title=Common mutations of ATP7B in Wilson disease patients from Hungary.
}}

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