{{Rsnum
|rsid=1559777
|Chromosome=15
|position=57788419
|Orientation=plus
|GMAF=0.2769
|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 | 69.0 | 25.7 | 5.3
| HCB | 67.9 | 27.0 | 5.1
| JPT | 45.1 | 45.1 | 9.7
| YRI | 19.0 | 55.8 | 25.2
| ASW | 19.6 | 64.3 | 16.1
| CHB | 67.9 | 27.0 | 5.1
| CHD | 59.6 | 33.9 | 6.4
| GIH | 65.3 | 30.7 | 4.0
| LWK | 31.8 | 49.1 | 19.1
| MEX | 60.3 | 36.2 | 3.4
| MKK | 34.2 | 47.7 | 18.1
| TSI | 67.6 | 30.4 | 2.0
| 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=1E-6
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}