{{Rsnum
|rsid=7823896
|Chromosome=8
|position=109205037
|Orientation=plus
|GMAF=0.2433
|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 | 0.9 | 23.4 | 75.7
| HCB | 0.7 | 11.8 | 87.5
| JPT | 1.8 | 9.7 | 88.5
| YRI | 52.4 | 44.4 | 3.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.7 | 11.8 | 87.5
| CHD | 0.0 | 8.3 | 91.7
| GIH | 3.0 | 37.6 | 59.4
| LWK | 0.0 | 0.0 | 0.0
| MEX | 3.5 | 22.8 | 73.7
| MKK | 37.8 | 45.9 | 16.2
| TSI | 2.9 | 28.4 | 68.6
| 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-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 | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}