{{Rsnum
|rsid=872863
|Gene=DENND1A
|Chromosome=9
|position=123392075
|Orientation=plus
|GMAF=0.0854
|Gene_s=DENND1A
|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 | 83.9 | 15.2 | 0.9
| HCB | 91.0 | 9.0 | 0.0
| JPT | 97.3 | 2.7 | 0.0
| YRI | 77.3 | 22.0 | 0.7
| ASW | 80.7 | 19.3 | 0.0
| CHB | 91.0 | 9.0 | 0.0
| CHD | 91.5 | 7.5 | 0.9
| GIH | 80.6 | 17.3 | 2.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 84.1 | 13.9 | 2.0
| TSI | 88.1 | 9.9 | 2.0
| 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-11
  |OR=NR
  |ORtxt=NR
  }}

{{PMID Auto
|PMID=20018028
|Title=Armitage's trend test for genome-wide association analysis: one-sided or two-sided?
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}