{{Rsnum
|rsid=10758892
|Chromosome=9
|position=7734250
|Orientation=plus
|GMAF=0.1079
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 90.3 | 9.7 | 0.0
| HCB | 85.4 | 14.6 | 0.0
| JPT | 75.2 | 22.1 | 2.7
| YRI | 49.7 | 44.9 | 5.4
| ASW | 63.2 | 35.1 | 1.8
| CHB | 85.4 | 14.6 | 0.0
| CHD | 86.1 | 13.9 | 0.0
| GIH | 87.1 | 11.9 | 1.0
| LWK | 64.5 | 30.9 | 4.5
| MEX | 84.5 | 15.5 | 0.0
| MKK | 66.0 | 32.1 | 1.9
| TSI | 90.2 | 9.8 | 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=9E-6
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}