{{Rsnum
|rsid=137853281
|Chromosome=13
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=ATP7B
|position=51942396
|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.52516532delG
|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=137853281
}}{{PMID Auto
|PMID=10994503
|Title=[Analysis of mutations and haplotypes of polymorphic markers in patients with Wilson-Konovalov disease from Bashkir].
}}

{{PMID Auto
|PMID=15024742
|Title=Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients.
}}

{{PMID Auto
|PMID=17897870
|Title=Neurological manifestations and ATP7B mutations in Wilson's disease.
}}

{{PMID Auto
|PMID=18855987
|Title=High frequency of the c.3207C>A (p.H1069Q) mutation in ATP7B gene of Lithuanian patients with hepatic presentation of Wilson's disease.
|OA=1
}}