{{Rsnum
|rsid=11723530
|Gene=FOXK1
|Chromosome=4
|position=169959732
|Orientation=plus
|GMAF=0.3039
|Gene_s=FOXK1
|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 | 32.3 | 43.5 | 24.2
| HCB | 0.0 | 10.9 | 89.1
| JPT | 0.0 | 9.7 | 90.3
| YRI | 0.7 | 27.2 | 72.1
| ASW | 7.1 | 21.4 | 71.4
| CHB | 0.0 | 10.9 | 89.1
| CHD | 0.9 | 13.0 | 86.1
| GIH | 0.0 | 0.0 | 0.0
| LWK | 3.6 | 26.4 | 70.0
| MEX | 15.5 | 55.2 | 29.3
| MKK | 4.6 | 32.7 | 62.7
| TSI | 0.0 | 0.0 | 0.0
| 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=4E-6
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}