{{Rsnum
|rsid=7323755
|Chromosome=13
|position=45326132
|Orientation=plus
|GMAF=0.06107
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 10.6 | 89.4
| HCB | 0.0 | 16.8 | 83.2
| JPT | 0.0 | 16.8 | 83.2
| YRI | 2.7 | 29.3 | 68.0
| ASW | 1.8 | 26.3 | 71.9
| CHB | 0.0 | 16.8 | 83.2
| CHD | 0.9 | 20.2 | 78.9
| GIH | 0.0 | 10.9 | 89.1
| LWK | 0.0 | 21.8 | 78.2
| MEX | 0.0 | 6.9 | 93.1
| MKK | 3.2 | 16.7 | 80.1
| TSI | 0.0 | 3.9 | 96.1
| 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-13
  |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}}