{{Rsnum
|rsid = 28934272
|Gene = OCA2
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=15
|position=27985101
|Gene_s=OCA2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=121918166
}}{{omim
| id = 203200
| variant = 0004
| desc    = ALBINISM, OCULOCUTANEOUS, TYPE II
| rsnum   = 28934272
}}
{{ neighbor
| rsid = 1800407
| distance = 71
}}

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

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