Barely Significant
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Association of lysyl oxidase-like 1 gene common sequence variants in Greek patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma.

Mol Vis · 2013 · PMC3712667 · PMID 23869164

Europe PMC
1
hedged sentence
0.0370
closest p · 0.7× alpha
0.0370
boldest claim

The sentences

nominally significantp=0.037actually significant
The combined haplotype GGT, consisting of all three risk alleles, was associated with PEX (p=0.037, nominally significant), conferring a 1.8-fold of increased risk of the disease (OR=1.8, 95% CI=1.03–3.28; Table 3 ).

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