{{Rsnum
|rsid=8050940
|Chromosome=16
|position=62066307
|Orientation=plus
|GMAF=0.0831
|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 | 0.0 | 3.6 | 96.4
| HCB | 0.0 | 7.3 | 92.7
| JPT | 0.0 | 16.8 | 83.2
| YRI | 10.4 | 40.3 | 49.3
| ASW | 8.8 | 38.6 | 52.6
| CHB | 0.0 | 7.3 | 92.7
| CHD | 0.0 | 7.3 | 92.7
| GIH | 0.0 | 5.0 | 95.0
| LWK | 4.6 | 39.4 | 56.0
| MEX | 0.0 | 7.0 | 93.0
| MKK | 2.6 | 45.8 | 51.6
| TSI | 0.0 | 9.8 | 90.2
| 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-26
  |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}}