{{Rsnum
|rsid=4792192
|Gene=DNAH9
|Chromosome=17
|position=11900144
|Orientation=plus
|GMAF=0.3035
|Gene_s=DNAH9
|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 | 2.7 | 15.9 | 81.4
| HCB | 17.5 | 43.8 | 38.7
| JPT | 8.8 | 41.6 | 49.6
| YRI | 48.3 | 42.9 | 8.8
| ASW | 29.8 | 49.1 | 21.1
| CHB | 17.5 | 43.8 | 38.7
| CHD | 11.0 | 52.3 | 36.7
| GIH | 7.9 | 42.6 | 49.5
| LWK | 60.0 | 36.4 | 3.6
| MEX | 0.0 | 24.1 | 75.9
| MKK | 43.6 | 44.2 | 12.2
| TSI | 0.0 | 25.5 | 74.5
| 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}}