{{Rsnum
|rsid=10053502
|Chromosome=5
|position=39979070
|Orientation=plus
|GMAF=0.073
|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 | 91.2 | 8.8 | 0.0
| HCB | 87.6 | 11.7 | 0.7
| JPT | 95.6 | 4.4 | 0.0
| YRI | 70.1 | 26.5 | 3.4
| ASW | 84.2 | 15.8 | 0.0
| CHB | 87.6 | 11.7 | 0.7
| CHD | 85.3 | 13.8 | 0.9
| GIH | 85.1 | 14.9 | 0.0
| LWK | 56.4 | 31.8 | 11.8
| MEX | 91.4 | 8.6 | 0.0
| MKK | 69.2 | 27.6 | 3.2
| TSI | 96.1 | 3.9 | 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-16
  |OR=NR
  |ORtxt=NR
  }}

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