{{Rsnum
|rsid=1800419
|Gene=OCA2
|Chromosome=15
|position=27851392
|Orientation=minus
|GMAF=0.4518
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=OCA2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 16.9 | 50.8 | 32.3
| HCB | 22.2 | 44.4 | 33.3
| JPT | 20.0 | 35.6 | 44.4
| YRI | 38.1 | 46.0 | 15.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 22.2 | 44.4 | 33.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=OCA2 GENE
|id=611409
|rsnum=1800419
}}

{{PMID Auto
|PMID=17236130
|Title=A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation.
|OA=1
}}

{{PMID Auto
|PMID=18392143
|Title=Interactions between SNP alleles at multiple loci contribute to skin color differences between caucasoid and mongoloid subjects.
|OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}