{{Rsnum
|rsid=11838472
|Chromosome=13
|position=73167012
|Orientation=plus
|GMAF=0.1667
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 92.0 | 8.0 | 0.0
| HCB | 55.5 | 35.8 | 8.8
| JPT | 61.1 | 28.3 | 10.6
| YRI | 51.7 | 42.2 | 6.1
| ASW | 64.9 | 29.8 | 5.3
| CHB | 55.5 | 35.8 | 8.8
| CHD | 47.2 | 38.0 | 14.8
| GIH | 53.5 | 39.6 | 6.9
| LWK | 57.3 | 36.4 | 6.4
| MEX | 77.6 | 20.7 | 1.7
| MKK | 75.5 | 23.2 | 1.3
| TSI | 98.0 | 2.0 | 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=3E-17
  |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}}