{{Rsnum
|rsid=72552255
|Chromosome=13
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ATP7B
|position=51946414
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=72552255
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=52520550
|CHROM=13
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050368000000040002100100
|GENEINFO=ATP7B:540
|GENE_NAME=ATP7B
|GENE_ID=540
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.52520550G>A
|CLNSRC=Emory University
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Wilson's disease; not provided
|Disease=Wilson's disease; not provided
|Tags=RV;PM;PMC;S3D;SLO;VLD;OTHERKG;LSD
|CLNACC=RCV000029359.1; RCV000078046.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1512:C0019202:277900:905:88518009
|CLNSRCID=6172
}}

{{PMID Auto
|PMID=98378
|Title=Differences in pituitary and testicular function between diabetic patients on insulin and oral anti-diabetic agents.
}}

{{PMID Auto
|PMID=11175281
|Title=Determination of the frequencies of ten allelic variants of the Wilson disease gene (ATP7B), in pooled DNA samples.
}}

{{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=17461475
|Title=Diagnostic criteria for acute liver failure due to Wilson disease.
}}

{{PMID Auto
|PMID=17717039
|Title=Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes.
|OA=1
}}

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

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