{{Rsnum
|rsid=193922103
|Chromosome=13
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ATP7B
|position=51958361
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922103
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=52532497
|CHROM=13
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.52532497T>C
|CLNSRC=Emory University
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Wilson's disease; not provided
|Disease=Wilson's disease; not provided
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000029355.1; RCV000078041.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1512:C0019202:277900:905:88518009
|GENEINFO=ATP7B:540
|GENE_ID=540
|GENE_NAME=ATP7B
|CLNSRCID=4555
}}{{PMID Auto
|PMID=169394
|Title=Denaturation map of polyoma DNA.
|OA=1
}}

{{PMID Auto
|PMID=9311736
|Title=Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses.
|OA=1
}}

{{PMID Auto
|PMID=10942420
|Title=Copper-dependent trafficking of Wilson disease mutant ATP7B proteins.
}}

{{PMID Auto
|PMID=11405812
|Title=Mutation analysis and the correlation between genotype and phenotype of Arg778Leu mutation in chinese patients with Wilson disease.
}}

{{PMID Auto
|PMID=14986826
|Title=Mutation spectrum and polymorphisms in ATP7B identified on direct sequencing of all exons in Chinese Han and Hui ethnic patients with Wilson's disease.
}}

{{PMID Auto
|PMID=19118915
|Title=Genotype-phenotype correlation in Italian children with Wilson's disease.
}}