{{Rsnum
|rsid=10500355
|Gene=RBFOX1
|Chromosome=16
|position=7409346
|Orientation=plus
|GMAF=0.2241
|Gene_s=RBFOX1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 10.6 | 42.5 | 46.9
| HCB | 0.7 | 11.7 | 87.6
| JPT | 0.9 | 9.7 | 89.4
| YRI | 1.4 | 23.8 | 74.8
| ASW | 5.3 | 38.6 | 56.1
| CHB | 0.7 | 11.7 | 87.6
| CHD | 0.9 | 13.0 | 86.1
| GIH | 2.0 | 30.7 | 67.3
| LWK | 3.6 | 30.0 | 66.4
| MEX | 6.9 | 48.3 | 44.8
| MKK | 4.5 | 34.0 | 61.5
| TSI | 10.8 | 51.0 | 38.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=23474815
|Title=Meta-Analysis of Genome-wide Association Studies in 5 cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}