{{Rsnum
|rsid=137853284
|Chromosome=13
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ATP7B
|position=51958334
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,C
|CHROM=13
|CLNALLE=2
|CLNDBN=Wilson's disease
|CLNDSDB=OMIM
|CLNDSDBID=277900
|CLNHGVS=NC_000013.10:g.52532470G>C
|CLNSIG=5
|Disease=Wilson's disease
|FwdALT=G,T
|FwdREF=C
|GENEINFO=ATP7B:540
|GENE_ID=540
|GENE_NAME=ATP7B
|REF=G
|RSPOS=52532470
|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=137853284
}}{{PMID Auto
|PMID=14974157
|Title=[ATP7B gene mutations in Hungarian patients with Wilson disease--case reports to illustrate the diverse clinical presentations].
}}

{{PMID Auto
|PMID=17160357
|Title=Analysis of most common mutations R778G, R778L, R778W, I1102T and H1069Q in Indian Wilson disease patients: correlation between genotype/phenotype/copper ATPase activity.
}}