{{Rsnum
|rsid=11223996
|Gene=HSFX1
|Chromosome=11
|position=134756993
|Orientation=plus
|GMAF=0.1056
|Gene_s=HSFX1
|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 | 1.8 | 27.7 | 70.5
| HCB | 0.0 | 15.2 | 84.8
| JPT | 0.0 | 6.2 | 93.8
| YRI | 0.7 | 9.1 | 90.2
| ASW | 0.0 | 19.6 | 80.4
| CHB | 0.0 | 15.2 | 84.8
| CHD | 1.9 | 17.0 | 81.1
| GIH | 0.0 | 5.0 | 95.0
| LWK | 0.0 | 9.4 | 90.6
| MEX | 3.5 | 17.5 | 78.9
| MKK | 1.3 | 16.9 | 81.8
| TSI | 4.9 | 22.5 | 72.5
| 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=7E-7
  |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}}