{{Rsnum
|rsid=16862782
|Gene=RFX3
|Chromosome=3
|position=187970102
|Orientation=plus
|GMAF=0.1276
|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 | 0.9 | 30.1 | 69.0
| HCB | 0.7 | 25.5 | 73.7
| JPT | 3.5 | 25.7 | 70.8
| YRI | 0.0 | 2.7 | 97.3
| ASW | 0.0 | 10.5 | 89.5
| CHB | 0.7 | 25.5 | 73.7
| CHD | 0.9 | 25.9 | 73.1
| GIH | 0.0 | 28.7 | 71.3
| LWK | 0.0 | 10.0 | 90.0
| MEX | 0.0 | 26.3 | 73.7
| MKK | 0.0 | 9.6 | 90.4
| TSI | 3.9 | 25.5 | 70.6
| 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=5E-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}}