{{Rsnum
|rsid=6841898
|Gene=DHX15
|Chromosome=4
|position=24576474
|Orientation=plus
|GMAF=0.05877
|Gene_s=DHX15
|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 | 97.3 | 2.7 | 0.0
| HCB | 91.9 | 8.1 | 0.0
| JPT | 86.7 | 13.3 | 0.0
| YRI | 79.9 | 18.1 | 2.1
| ASW | 78.9 | 17.5 | 3.5
| CHB | 91.9 | 8.1 | 0.0
| CHD | 92.7 | 7.3 | 0.0
| GIH | 91.0 | 9.0 | 0.0
| LWK | 82.7 | 17.3 | 0.0
| MEX | 89.7 | 10.3 | 0.0
| MKK | 71.1 | 27.0 | 2.0
| TSI | 94.1 | 4.9 | 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=3E-26
  |OR=NR
  |ORtxt=NR
  }}

{{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}}