{{Rsnum
|rsid=11618212
|Chromosome=13
|position=105444463
|Orientation=plus
|GMAF=0.152
|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 | 55.8 | 38.9 | 5.3
| HCB | 77.8 | 20.7 | 1.5
| JPT | 77.8 | 22.2 | 0.0
| YRI | 85.7 | 12.7 | 1.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 77.8 | 20.7 | 1.5
| CHD | 76.4 | 23.6 | 0.0
| GIH | 47.0 | 45.0 | 8.0
| LWK | 92.4 | 7.6 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 89.0 | 11.0 | 0.0
| TSI | 64.6 | 31.3 | 4.0
| 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=5E-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 | FTDNA}}
{{on chip | Illumina Human 1M}}