Barely Significant
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Association of <i>FOXE3</i>-p.Ala170Ala and <i>PITX3</i>-p.Ile95Ile Polymorphisms with Congenital Cataract and Microphthalmia.

J Ophthalmic Vis Res · 2018 · PMC6210873 · PMID 30479708

Europe PMCDOI
1
hedged sentence
0.0115
closest p · 0.2× alpha
0.0115
boldest claim

The sentences

borderline significanceP = 0.0115actually significant
Results: A significantly high frequency of T allele and a borderline significance in the frequency of TT genotype of FOXE3 -p.Ala170Ala was observed in microphthalmia cases, as compared to controls [T allele: OR: [CI] = 1.8 [1.15-2.72], P = 0.0115; TT: OR [CI] = 2.9 [1.14-7.16], P = 0.0291).

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