{{Rsnum
|rsid=1656966
|Chromosome=3
|position=186748463
|Orientation=minus
|GMAF=0.197
|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 | 70.5 | 28.6 | 0.9
| HCB | 40.9 | 51.1 | 8.0
| JPT | 39.8 | 54.0 | 6.2
| YRI | 58.9 | 36.3 | 4.8
| ASW | 59.6 | 36.8 | 3.5
| CHB | 40.9 | 51.1 | 8.0
| CHD | 45.9 | 41.3 | 12.8
| GIH | 0.0 | 0.0 | 0.0
| LWK | 78.9 | 19.3 | 1.8
| MEX | 74.1 | 25.9 | 0.0
| MKK | 79.5 | 19.2 | 1.3
| TSI | 74.3 | 23.8 | 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=4E-21
  |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}}