{{Rsnum
|rsid=2267138
|Chromosome=22
|position=29397652
|Orientation=plus
|GMAF=0.1745
|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 | 76.1 | 23.0 | 0.9
| HCB | 43.1 | 43.8 | 13.1
| JPT | 35.5 | 50.9 | 13.6
| YRI | 81.0 | 18.4 | 0.7
| ASW | 77.2 | 21.1 | 1.8
| CHB | 43.1 | 43.8 | 13.1
| CHD | 51.9 | 38.9 | 9.3
| GIH | 82.2 | 16.8 | 1.0
| LWK | 88.2 | 11.8 | 0.0
| MEX | 79.3 | 19.0 | 1.7
| MKK | 68.6 | 28.2 | 3.2
| TSI | 74.3 | 25.7 | 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=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}}