{{Rsnum
|rsid=193922111
|Chromosome=13
|Orientation=minus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=ATP7B
|position=51974375
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922111
|Reversed=1
|FwdREF=T
|FwdALT=
|REF=GA
|ALT=G
|RSPOS=52548510
|CHROM=13
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.52548511delA
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Wilson's disease
|Disease=Wilson's disease
|Tags=RV;PM;PMC;OTHERKG;LSD
|CLNACC=RCV000029384.1
|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=1124372
|Title=[Psychodiagnostic factors of indication for abortion].
}}

{{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=9801873
|Title=Haplotype and mutation analysis in Greek patients with Wilson disease.
}}

{{PMID Auto
|PMID=11216666
|Title=Delineation of the spectrum of Wilson disease mutations in the Greek population and the identification of six novel mutations.
}}

{{PMID Auto
|PMID=15523622
|Title=Genotype-phenotype correlations for a wide spectrum of mutations in the Wilson disease gene (ATP7B).
}}

{{PMID Auto
|PMID=19172127
|Title=Wilson disease in children: analysis of 57 cases.
}}