rs17648524, RBFOX1

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hyperopia
CUI: C0020490
Disease: Hyperopia
0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. 25233373 2014
Abnormality of refraction
CUI: C4025843
Disease: Abnormality of refraction
0.700 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134 2013
Refractive Errors
CUI: C0034951
Disease: Refractive Errors
0.700 GeneticVariation GWASDB Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134 2013
Severe myopia
CUI: C0271183
Disease: Severe myopia
0.010 GeneticVariation BEFREE Our findings suggested rs17648524 (intronic RBFOX1 gene) and rs7084402 (7.5kb 5' of the BICC1 gene) showed gender-specific associations with high myopia in the Han Chinese. 28085524 2017