{{Rsnum
|rsid=1668357
|Chromosome=7
|position=37964804
|Orientation=minus
|GMAF=0.1754
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 81.5 | 18.5 | 0.0
| HCB | 22.2 | 57.8 | 20.0
| JPT | 11.1 | 64.4 | 24.4
| YRI | 74.1 | 25.2 | 0.7
| ASW | 74.5 | 20.0 | 5.5
| CHB | 22.2 | 57.8 | 20.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 71.8 | 27.3 | 0.9
| MEX | 0.0 | 0.0 | 0.0
| MKK | 76.8 | 22.5 | 0.7
| TSI | 0.0 | 0.0 | 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=4E-8
  |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}}