Barely Significant
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Genome-wide association study of the common retinal disorder epiretinal membrane: Significant risk loci in each of three American populations.

Cell Genom · 2024 · PMC11228954 · PMID 38870908

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nominally significantno p-value reported
For EUR, of the 28 loci available for lookup in FinnGen, 25 had concordant direction of effect, 20 were nominally significant (<0.05), 14 survived Bonferroni correction (for 28 tests; 0.05/28 = 0.0018), and 4 were independently GWS.

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