{{Rsnum
|rsid=121907990
|Chromosome=13
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ATP7B
|position=51937570
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATP7B
}}{{omim
|id=606882
|rsnum=121907990
|variant=0003
}}
{{omim
|id=606882
|rsnum=121907990
|variant=0017
}}{{ClinVar
|rsid=121907990
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=52511706
|CHROM=13
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ATP7B:540
|GENE_NAME=ATP7B
|GENE_ID=540
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.52511706T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606882.0003; 606882.0017
|CLNSIG=5
|CLNCUI=C0019202
|CLNDBN=Wilson's disease
|Disease=Wilson's disease
|CLNACC=RCV000004063.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1512:C0019202:277900:905:88518009
}}