{{Rsnum
|rsid=60986317
|Gene=ATP7B
|Chromosome=13
|position=51934853
|Orientation=plus
|GMAF=0.001377
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|rsid=60986317
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=52508989
|CHROM=13
|GMAF=0.0014
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050178000000040016100100
|GENEINFO=ATP7B:540
|GENE_NAME=ATP7B
|GENE_ID=540
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.52508989G>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Wilson's disease
|Disease=Wilson's disease
|Tags=PM;TPA;PMC;SLO;VLD;KGPhase1;KGPROD;OTHERKG;LSD
|CAF=0.9986; 0.001377
|CLNACC=RCV000029379.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1512:C0019202:277900:905:88518009
|COMMON=0
}}

{{PMID Auto
|PMID=10544227
|Title=Mutation analysis in patients of Mediterranean descent with Wilson disease: identification of 19 novel mutations.
|OA=1
}}

{{PMID Auto
|PMID=14962673
|Title=Functional assessment of the carboxy-terminus of the Wilson disease copper-transporting ATPase, ATP7B.
}}

{{PMID Auto
|PMID=18483695
|Title=Mutational analysis of ATP7B gene in Egyptian children with Wilson disease: 12 novel mutations.
}}

{{PMID Auto
|PMID=21454443
|Title=Critical roles for the COOH terminus of the Cu-ATPase ATP7B in protein stability, trans-Golgi network retention, copper sensing, and retrograde trafficking.
|OA=1
}}

{{PMID Auto
|PMID=21682854
|Title=Phenotypic and genetic characterization of a cohort of pediatric Wilson disease patients.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}