rs12051285 - RBFOX1
Magnitude 2.2 · 1 study on file
Reported associations
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Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci - Unknown journal (n.d.) · Unknown authors · PubMed 30306274
ABSTRACT: Previous studies have suggested that naturally occurring genetic variation contributes to the risk of astigmatism. The purpose of this investigation was to identify genetic markers associated with corneal and refractive astigmatism in a large-scale European ancestry cohort (UK Biobank) who underwent keratometry and autorefraction at an assessment centre. Genome-wide association studies for corneal and refractive astigmatism were performed in individuals of European ancestry (N = 86,335 and 88,005 respectively), with the mean corneal astigmatism or refractive astigmatism in fellow eyes analysed as a quantitative trait (dependent variable). Genetic correlation between the two traits was calculated using LD Score regression. Gene-based and gene-set tests were carried out using M
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Discuss with your doctor
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Genetic astigmatism risk with eye care provider Moderate
RBFOX1 rs12051285 G allele associated with refractive astigmatism risk
Inform ophthalmologist or optometrist of genetic predisposition at next visit
Screening
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Vision screening for astigmatism Moderate
RBFOX1 rs12051285 G allele carriers have increased risk of refractive astigmatism
Annual or biennial comprehensive eye exams to assess for refractive astigmatism