{{Rsnum
|rsid=17183295
|Gene=MYO1D
|Chromosome=17
|position=32751254
|Orientation=plus
|GMAF=0.0955
|Gene_s=MYO1D
|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 | 71.7 | 25.7 | 2.7
| HCB | 97.8 | 2.2 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 99.3 | 0.7 | 0.0
| ASW | 82.5 | 17.5 | 0.0
| CHB | 97.8 | 2.2 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 45.5 | 43.6 | 10.9
| LWK | 96.3 | 3.7 | 0.0
| MEX | 77.6 | 17.2 | 5.2
| MKK | 85.8 | 14.2 | 0.0
| TSI | 60.8 | 33.3 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23396134
  |Trait=Refractive error
  |Title=Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
  |RiskAllele=T
  |Pval=1E-10
  |OR=.13
  |ORtxt=[0.092-0.17] unit decrease
  |OA=1
}}

{{on chip | Affy GenomeWide 6}}