{{Rsnum
|rsid=1254319
|Gene=C14orf39
|Chromosome=14
|position=60437039
|Orientation=plus
|GMAF=0.4371
|Gene_s=C14orf39
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 10.0 | 38.2 | 51.8
| HCB | 39.4 | 46.0 | 14.6
| JPT | 38.1 | 49.6 | 12.4
| YRI | 29.2 | 52.8 | 18.1
| ASW | 21.1 | 49.1 | 29.8
| CHB | 39.4 | 46.0 | 14.6
| CHD | 46.8 | 40.4 | 12.8
| GIH | 25.7 | 49.5 | 24.8
| LWK | 24.5 | 50.0 | 25.5
| MEX | 5.3 | 47.4 | 47.4
| MKK | 28.8 | 53.8 | 17.3
| TSI | 16.7 | 44.1 | 39.2
| 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=A
  |Pval=1E-8
  |OR=.09
  |ORtxt=[0.059-0.117] unit decrease
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}