Variant: rs10500355

present in Gene: RBFOX1 present in Chromosome: 16 Position on Chromosome: 7409346 Alleles of this Variant: T/A

rs10500355 in RBFOX1 gene and Abnormality of refraction PMID 23474815 2013 Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.

rs10500355 in RBFOX1 gene and Myopia PMID 27182965 2016 Detection and interpretation of shared genetic influences on 42 human traits.

rs10500355 in RBFOX1 gene and Refractive Errors PMID 23474815 2013 Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.