{{Rsnum
|rsid=4737395
|Chromosome=8
|position=55686989
|Orientation=plus
|GMAF=0.1263
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 77.0 | 21.2 | 1.8
| HCB | 79.6 | 20.4 | 0.0
| JPT | 72.6 | 23.9 | 3.5
| YRI | 79.5 | 18.5 | 2.1
| ASW | 86.0 | 14.0 | 0.0
| CHB | 79.6 | 20.4 | 0.0
| CHD | 86.2 | 13.8 | 0.0
| GIH | 69.3 | 28.7 | 2.0
| LWK | 85.5 | 12.7 | 1.8
| MEX | 58.6 | 34.5 | 6.9
| MKK | 61.5 | 36.5 | 1.9
| TSI | 87.3 | 12.7 | 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=5E-9
  |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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}