{{Rsnum
|rsid=137853280
|Chromosome=13
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ATP7B
|position=51965034
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=606882
|variant=0008
|rsnum=137853280
}}{{ClinVar
|rsid=137853280
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=52539170
|CHROM=13
|dbSNPBuildID=133
|SSR=0
|SAO=0
|VP=0x050068000000000002110100
|GENEINFO=ATP7B:540
|GENE_NAME=ATP7B
|GENE_ID=540
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.52539170C>G
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606882.0008
|CLNSIG=5
|CLNCUI=C0019202
|CLNDBN=Wilson's disease
|Disease=Wilson's disease
|CLNACC=RCV000004054.1
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1512:C0019202:277900:905:88518009
}}{{PMID Auto
|PMID=7626145
|Title=The Wilson disease gene: spectrum of mutations and their consequences.
}}

{{PMID Auto
|PMID=11060541
|Title=Severe hepatic Wilson's disease in preschool-aged children.
}}

{{PMID Auto
|PMID=18760268
|Title=Rapid diagnosis of Wilson disease by a 28-mutation panel: real-time amplification refractory mutation system in diagnosing acute Wilsonian liver failure.
}}

{{PMID Auto
|PMID=18841564
|Title=[Mutation screening and prenatal diagnosis of Wilson's disease by denature high performance liquid chromatography].
}}