{{Rsnum
|rsid=7744813
|Gene=KCNQ5
|Chromosome=6
|position=72933566
|Orientation=plus
|GMAF=0.2851
|Gene_s=KCNQ5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 37.2 | 50.4 | 12.4
| HCB | 70.8 | 26.3 | 2.9
| JPT | 54.9 | 35.4 | 9.7
| YRI | 61.2 | 34.7 | 4.1
| ASW | 64.9 | 28.1 | 7.0
| CHB | 70.8 | 26.3 | 2.9
| CHD | 74.1 | 22.2 | 3.7
| GIH | 35.6 | 50.5 | 13.9
| LWK | 77.3 | 20.9 | 1.8
| MEX | 45.6 | 45.6 | 8.8
| MKK | 77.6 | 19.2 | 3.2
| TSI | 35.3 | 42.2 | 22.5
| 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-9
  |OR=.11
  |ORtxt=[0.075-0.149] unit increase
  |OA=1
}}

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