{{Rsnum
|rsid=656319
|Chromosome=8
|position=9956901
|Orientation=plus
|GMAF=0.4128
|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 | 33.6 | 53.1 | 13.3
| HCB | 0.0 | 7.3 | 92.7
| JPT | 2.7 | 23.0 | 74.3
| YRI | 16.3 | 50.3 | 33.3
| ASW | 31.6 | 43.9 | 24.6
| CHB | 0.0 | 7.3 | 92.7
| CHD | 0.0 | 5.6 | 94.4
| GIH | 14.9 | 50.5 | 34.7
| LWK | 24.5 | 54.5 | 20.9
| MEX | 22.4 | 41.4 | 36.2
| MKK | 23.1 | 46.8 | 30.1
| TSI | 40.2 | 46.1 | 13.7
| 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 | Illumina Human 1M}}