{{Rsnum
|rsid=1302019
|Chromosome=6
|position=147650438
|Orientation=minus
|GMAF=0.0528
|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 | 94.7 | 5.3 | 0.0
| HCB | 76.6 | 22.6 | 0.7
| JPT | 77.9 | 20.4 | 1.8
| YRI | 96.6 | 3.4 | 0.0
| ASW | 90.7 | 9.3 | 0.0
| CHB | 76.6 | 22.6 | 0.7
| CHD | 78.0 | 21.1 | 0.9
| GIH | 97.0 | 3.0 | 0.0
| LWK | 92.7 | 7.3 | 0.0
| MEX | 93.1 | 6.9 | 0.0
| MKK | 97.4 | 2.6 | 0.0
| TSI | 97.1 | 2.9 | 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=2E-23
  |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}}