{{Rsnum
|rsid=193922107
|Chromosome=13
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ATP7B
|position=51939091
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922107
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=52513227
|CHROM=13
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.52513227G>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Wilson's disease
|Disease=Wilson's disease
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000029374.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1512:C0019202:277900:905:88518009
|GENEINFO=ATP7B:540
|GENE_ID=540
|GENE_NAME=ATP7B
}}{{PMID Auto
|PMID=19118
|Title=Studies on the cardiovascular effects of pindolol in DOCA/saline hypertensive rats.
|OA=1
}}

{{PMID Auto
|PMID=10447265
|Title=Mutation analysis in patients with Wilson disease: identification of 4 novel mutations. Mutation in brief no. 250. Online.
}}

{{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=16283883
|Title=Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease.
}}

{{PMID Auto
|PMID=16684691
|Title=Familial gene analysis for Wilson disease from north-west Indian patients.
}}

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