rs11942256 - BMP3
Magnitude 2.8 · 1 study on file
Reported associations
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Insights into the genetic basis of retinal detachment - Unknown journal (n.d.) · Unknown authors · PubMed 31816047
ABSTRACT: Abstract Retinal detachment (RD) is a serious and common condition, but genetic studies to date have been hampered by the small size of the assembled cohorts. In the UK Biobank data set, where RD was ascertained by self-report or hospital records, genetic correlations between RD and high myopia or cataract operation were, respectively, 0.46 (SE = 0.08) and 0.44 (SE = 0.07). These correlations are consistent with known epidemiological associations. Through meta-analysis of genome-wide association studies using UK Biobank RD cases (N = 3 977) and two cohorts, each comprising ~1 000 clinically ascertained rhegmatogenous RD patients, we uncovered 11 genome-wide significant association signals. These are near or within ZC3H11B, BMP3, COL22A1, DLG5, PLCE1, EFEMP2, TYR, F
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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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discuss retinal detachment risk with ophthalmologist Moderate
BMP3 variants identified through GWAS in 364k individuals show association with retinal detachment
Inform eye care provider of genetic predisposition at routine visit
Screening
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ophthalmic examination for retinal detachment risk assessment Moderate
BMP3 genetic variants show association with retinal detachment and retinal breaks in large cohort study
Annual comprehensive eye examination with emphasis on retinal evaluation