Barely Significant
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The MYLIP p.N342S polymorphism is associated with response to lipid-lowering therapy in Brazilian patients with familial hypercholesterolemia.

Pharmacogenet Genomics · 2014 · PMC4206345 · PMID 25171759

Europe PMCDOI
1
hedged sentence
0.0600
closest p · 1.2× alpha
0.0600
boldest claim

The sentences

marginally significantP =0.06so close (0.05 < p ≤ 0.1)
Interestingly, the association between the MYLIP genotype and the presence or absence of an LDLR mutation was marginally significant ( P =0.06).

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.