{{Rsnum
|rsid=12525668
|Chromosome=6
|position=107696467
|Orientation=plus
|GMAF=0.07943
|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 | 81.4 | 18.6 | 0.0
| HCB | 79.1 | 19.4 | 1.5
| JPT | 88.3 | 10.8 | 0.9
| YRI | 100.0 | 0.0 | 0.0
| ASW | 96.5 | 3.5 | 0.0
| CHB | 79.1 | 19.4 | 1.5
| CHD | 80.4 | 16.8 | 2.8
| GIH | 82.2 | 15.8 | 2.0
| LWK | 96.4 | 3.6 | 0.0
| MEX | 53.4 | 41.4 | 5.2
| MKK | 98.1 | 1.9 | 0.0
| TSI | 88.2 | 11.8 | 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=8E-11
  |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}}