{{Rsnum
|rsid=9984974
|Chromosome=21
|position=36437079
|Orientation=plus
|GMAF=0.3205
|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 | 75.2 | 23.0 | 1.8
| HCB | 31.4 | 48.9 | 19.7
| JPT | 46.0 | 40.7 | 13.3
| YRI | 12.9 | 46.3 | 40.8
| ASW | 26.3 | 47.4 | 26.3
| CHB | 31.4 | 48.9 | 19.7
| CHD | 25.7 | 45.9 | 28.4
| GIH | 31.7 | 50.5 | 17.8
| LWK | 21.8 | 51.8 | 26.4
| MEX | 53.4 | 41.4 | 5.2
| MKK | 31.4 | 46.8 | 21.8
| TSI | 73.5 | 25.5 | 1.0
| 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=2E-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 | Illumina Human 1M}}