{{Rsnum
|rsid=138427376
|Gene=ATP7B
|Chromosome=13
|position=51968544
|Orientation=plus
|GMAF=0.003673
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|rsid=138427376
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=52542680
|CHROM=13
|GMAF=0.0037
|dbSNPBuildID=134
|SSR=0
|SAO=1
|VP=0x050268000000000416100100
|GENEINFO=ATP7B:540
|GENE_NAME=ATP7B
|GENE_ID=540
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.52542680A>G
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Wilson's disease
|Disease=Wilson's disease
|Tags=PM;PMC;S3D;HD;KGPhase1;KGPROD;OTHERKG;LSD
|CAF=0.9963; 0.003673
|CLNACC=RCV000029352.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1512:C0019202:277900:905:88518009
|COMMON=1
}}{{PMID Auto
|PMID=18373411
|Title=New mutations in the Wilson disease gene, ATP7B: implications for molecular testing.
}}