{{Rsnum
|rsid=13201929
|Chromosome=6
|position=117284828
|Orientation=plus
|GMAF=0.1019
|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 | 3.5 | 26.5 | 69.9
| HCB | 2.9 | 32.1 | 65.0
| JPT | 1.8 | 23.9 | 74.3
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 5.3 | 94.7
| CHB | 2.9 | 32.1 | 65.0
| CHD | 3.7 | 23.9 | 72.5
| GIH | 0.0 | 22.2 | 77.8
| LWK | 0.0 | 4.7 | 95.3
| MEX | 0.0 | 12.1 | 87.9
| MKK | 1.3 | 9.7 | 89.0
| TSI | 1.0 | 21.8 | 77.2
| 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-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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}