{{Rsnum
|rsid=10503019
|Gene=ATP8B1
|Chromosome=18
|position=57787145
|Orientation=plus
|GMAF=0.1483
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ATP8B1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 4.4 | 38.1 | 57.5
| HCB | 0.0 | 16.8 | 83.2
| JPT | 0.0 | 15.0 | 85.0
| YRI | 0.0 | 2.7 | 97.3
| ASW | 0.0 | 7.0 | 93.0
| CHB | 0.0 | 16.8 | 83.2
| CHD | 2.8 | 18.3 | 78.9
| GIH | 4.0 | 27.7 | 68.3
| LWK | 0.9 | 8.2 | 90.9
| MEX | 3.4 | 34.5 | 62.1
| MKK | 1.9 | 20.1 | 77.9
| TSI | 4.9 | 28.4 | 66.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19890347
|Trait=Vitiligo
|Title=Genome-Wide Association Study of Generalized Vitiligo in an Isolated European Founder Population Identifies SMOC2, in Close Proximity to IDDM8
|RiskAllele=
|Pval=0.000003
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10503019
|overall_frequency_n=13
|overall_frequency_d=128
|overall_frequency=0.101562
|n_genomes=11
|n_genomes_annotated=0
|n_haplomes=12
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}