{{Rsnum
|rsid=121907998
|Chromosome=13
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ATP7B
|position=51961849
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATP7B
}}{{omim
|id=606882
|rsnum=121907998
|variant=0020
}}{{ClinVar
|rsid=121907998
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=52535985
|CHROM=13
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=ATP7B:540
|GENE_NAME=ATP7B
|GENE_ID=540
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.52535985A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606882.0020
|CLNSIG=5
|CLNCUI=C0019202
|CLNDBN=Wilson's disease
|Disease=Wilson's disease
|CLNACC=RCV000004066.1
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1512:C0019202:277900:905:88518009
}}{{PMID Auto
|PMID=1502474
|Title=[Dental implants. The contribution of iliac bone grafts].
}}

{{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=9482578
|Title=Novel ATP7B mutations causing Wilson disease in several Israeli ethnic groups.
}}

{{PMID Auto
|PMID=15994426
|Title=NH2-terminal signals in ATP7B Cu-ATPase mediate its Cu-dependent anterograde traffic in polarized hepatic cells.
}}

{{PMID Auto
|PMID=16233999
|Title=Wilson's Disease.
}}

{{PMID Auto
|PMID=17433323
|Title=Late-onset Wilson's disease.
}}