{{Rsnum
|rsid=7939886
|Chromosome=11
|position=56474785
|Orientation=plus
|GMAF=0.1185
|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 | 76.8 | 21.4 | 1.8
| HCB | 77.9 | 20.6 | 1.5
| JPT | 74.1 | 25.9 | 0.0
| YRI | 85.0 | 14.3 | 0.7
| ASW | 82.5 | 15.8 | 1.8
| CHB | 77.9 | 20.6 | 1.5
| CHD | 77.4 | 22.6 | 0.0
| GIH | 77.2 | 21.8 | 1.0
| LWK | 76.6 | 23.4 | 0.0
| MEX | 85.7 | 10.7 | 3.6
| MKK | 75.6 | 23.7 | 0.6
| TSI | 83.3 | 15.7 | 1.0
| 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=2E-7
  |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}}