{{Rsnum
|rsid=6111803
|Gene=OVOL2
|Chromosome=20
|position=18041718
|Orientation=plus
|GMAF=0.03444
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=OVOL2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 83.2 | 15.0 | 1.8
| HCB | 99.3 | 0.7 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 86.4 | 12.9 | 0.7
| ASW | 84.2 | 15.8 | 0.0
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 97.0 | 3.0 | 0.0
| LWK | 88.2 | 11.8 | 0.0
| MEX | 94.8 | 5.2 | 0.0
| MKK | 96.8 | 3.2 | 0.0
| TSI | 92.2 | 7.8 | 0.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19574904
|Title=Exclusion of Positional Candidate Gene Coding Region Mutations in the Common Posterior Polymorphous Corneal Dystrophy 1 Candidate Gene Interval
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}