{{Rsnum
|rsid=137853283
|Chromosome=13
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ATP7B
|position=51958330
|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.52532466C>T
|CLNSIG=5
|Disease=Wilson's disease
|FwdALT=A
|FwdREF=G
|GENEINFO=ATP7B:540
|GENE_ID=540
|GENE_NAME=ATP7B
|REF=C
|RSPOS=52532466
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;S3D;NSN;REF;INT;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050268080601000002110100
|WGT=1
|dbSNPBuildID=133
|rsid=137853283
}}{{PMID Auto
|PMID=11690702
|Title=High prevalence of the H1069Q mutation in East German patients with Wilson disease: rapid detection of mutations by limited sequencing and phenotype-genotype analysis.
}}

{{PMID Auto
|PMID=15202786
|Title=Rapid detection of mutations in Wilson disease gene ATP7B by DNA strip technology.
}}