{{Rsnum
|rsid=3138144
|Gene=RDH5
|Chromosome=12
|position=55720985
|Orientation=minus
|GMAF=0.3714
|Gene_s=RDH5,RPL12P34
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 38.1 | 41.6 | 20.4
| HCB | 26.3 | 59.1 | 14.6
| JPT | 37.2 | 41.6 | 21.2
| YRI | 87.8 | 10.9 | 1.4
| ASW | 63.2 | 33.3 | 3.5
| CHB | 26.3 | 59.1 | 14.6
| CHD | 24.8 | 50.5 | 24.8
| GIH | 18.8 | 49.5 | 31.7
| LWK | 80.0 | 19.1 | 0.9
| MEX | 31.0 | 44.8 | 24.1
| MKK | 55.1 | 39.7 | 5.1
| TSI | 31.7 | 45.5 | 22.8
| 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=C
  |Pval=4E-12
  |OR=.12
  |ORtxt=[0.086-0.152] unit increase
  |OA=1
}}

{{PMID Auto
|PMID=20668683
|Title=Genetically dependent ERBB3 expression modulates antigen presenting cell function and type 1 diabetes risk.
|OA=1
}}

{{on chip | Affy GenomeWide 6}}