{{Rsnum
|rsid=7077335
|Chromosome=10
|position=6315794
|Orientation=plus
|GMAF=0.1878
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 98.2 | 1.8 | 0.0
| HCB | 60.6 | 34.3 | 5.1
| JPT | 61.9 | 31.9 | 6.2
| YRI | 21.8 | 40.1 | 38.1
| ASW | 29.8 | 45.6 | 24.6
| CHB | 60.6 | 34.3 | 5.1
| CHD | 65.7 | 32.4 | 1.9
| GIH | 98.0 | 2.0 | 0.0
| LWK | 21.8 | 50.0 | 28.2
| MEX | 91.4 | 8.6 | 0.0
| MKK | 30.0 | 53.3 | 16.7
| TSI | 99.0 | 1.0 | 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=2E-12
  |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}}