{{Rsnum
|rsid=1061472
|Gene=ATP7B
|Chromosome=13
|position=51950352
|Orientation=minus
|GMAF=0.4927
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 19.5 | 50.4 | 30.1
| HCB | 36.0 | 50.7 | 13.2
| JPT | 49.5 | 36.0 | 14.4
| YRI | 22.1 | 59.3 | 18.6
| ASW | 36.8 | 50.9 | 12.3
| CHB | 36.0 | 50.7 | 13.2
| CHD | 31.5 | 50.9 | 17.6
| GIH | 34.7 | 45.5 | 19.8
| LWK | 29.4 | 49.5 | 21.1
| MEX | 25.9 | 48.3 | 25.9
| MKK | 38.1 | 41.3 | 20.6
| TSI | 17.6 | 44.1 | 38.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=22356903
|Title=Association of K832R and R952K SNPs of Wilson's Disease Gene with Alzheimer's Disease
}}

{{ClinVar
|rsid=1061472
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=52524488
|CHROM=13
|GMAF=0.4931
|dbSNPBuildID=86
|SSR=0
|SAO=1
|VP=0x05037800000017051f100101
|GENEINFO=ATP7B:540
|GENE_NAME=ATP7B
|GENE_ID=540
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.52524488T>C
|CLNSRC=Emory University
|CLNORIGIN=1
|CLNSIG=2
|CLNDBN=Wilson's disease; AllHighlyPenetrant
|Disease=Wilson's disease; AllHighlyPenetrant
|Tags=RV;PM;TPA;PMC;S3D;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD
|CAF=0.5073; 0.4927
|CLNACC=RCV000029356.1; RCV000078043.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1512:C0019202:277900:905:88518009; CN169374
|COMMON=1
|CLNSRCID=4452
}}

{{PMID|11405812}} Mutation analysis and the correlation between genotype and phenotype of Arg778Leu mutation in chinese patients with Wilson disease.

{{GET Evidence
|gene=ATP7B
|aa_change=Lys832Arg
|aa_change_short=K832R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1061472
|overall_frequency_n=5812
|overall_frequency_d=10468
|overall_frequency=0.555216
|n_genomes=46
|n_genomes_annotated=0
|n_haplomes=58
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=3
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|pph2_score=0.461
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=-3
|autoscore=3
|n_web_uneval=7
}}

{{PMID Auto
|PMID=24852429
|Title=The ATP7B genetic polymorphisms predict clinical outcome to platinum-based chemotherapy in lung cancer patients
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}