{{Rsnum
|rsid=41292782
|Gene=ATP7B
|Chromosome=13
|position=51946372
|Orientation=plus
|GMAF=0.0009183
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|rsid=41292782
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=52520508
|CHROM=13
|GMAF=0.0009
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050268000000040116100100
|GENEINFO=ATP7B:540
|GENE_NAME=ATP7B
|GENE_ID=540
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.52520508G>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Wilson's disease
|Disease=Wilson's disease
|Tags=PM;PMC;S3D;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD
|CAF=0.9991; 0.0009183
|CLNACC=RCV000029361.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1512:C0019202:277900:905:88518009
|COMMON=0
}}

{{PMID Auto
|PMID=16088907
|Title=Twenty-four novel mutations in Wilson disease patients of predominantly European ancestry.
}}

{{PMID Auto
|PMID=17949296
|Title=Twenty-four novel mutations in Wilson disease patients of predominantly Italian origin.
}}

{{PMID Auto
|PMID=20333758
|Title=Functional analysis of mutations in the ATP loop of the Wilson disease copper transporter, ATP7B.
}}

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