{{Rsnum
|rsid=13172324
|Chromosome=5
|position=7368732
|Orientation=plus
|GMAF=0.03673
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 78.0 | 21.1 | 0.9
| HCB | 92.7 | 6.6 | 0.7
| JPT | 98.2 | 1.8 | 0.0
| YRI | 83.7 | 15.0 | 1.4
| ASW | 87.3 | 12.7 | 0.0
| CHB | 92.7 | 6.6 | 0.7
| CHD | 97.2 | 2.8 | 0.0
| GIH | 86.1 | 11.9 | 2.0
| LWK | 87.3 | 11.8 | 0.9
| MEX | 91.4 | 8.6 | 0.0
| MKK | 86.5 | 12.8 | 0.6
| TSI | 87.6 | 11.3 | 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=3E-10
  |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 | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}