{{Rsnum
|rsid=1944866
|Chromosome=11
|position=134612572
|Orientation=plus
|GMAF=0.2144
|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 | 1.6 | 11.5 | 86.9
| HCB | 8.0 | 41.6 | 50.4
| JPT | 0.0 | 32.7 | 67.3
| YRI | 12.9 | 51.0 | 36.1
| ASW | 10.7 | 35.7 | 53.6
| CHB | 8.0 | 41.6 | 50.4
| CHD | 5.6 | 51.9 | 42.6
| GIH | 0.0 | 0.0 | 0.0
| LWK | 18.2 | 45.5 | 36.4
| MEX | 1.8 | 26.8 | 71.4
| MKK | 8.7 | 39.6 | 51.7
| 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=2E-6
  |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 | Illumina Human 1M}}