{{Rsnum
|rsid=6472235
|Chromosome=8
|position=65909795
|Orientation=plus
|GMAF=0.3967
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 15.6 | 43.8 | 40.6
| HCB | 0.7 | 18.2 | 81.0
| JPT | 3.5 | 24.8 | 71.7
| YRI | 80.7 | 18.6 | 0.7
| ASW | 55.4 | 35.7 | 8.9
| CHB | 0.7 | 18.2 | 81.0
| CHD | 2.8 | 18.3 | 78.9
| GIH | 2.0 | 25.5 | 72.4
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 54.2 | 42.6 | 3.2
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23049088
  |Trait=Myopia (pathological)
  |Title=A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
  |RiskAllele=
  |Pval=1E-7
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}