Barely Significant
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CNOT3 is a modifier of PRPF31 mutations in retinitis pigmentosa with incomplete penetrance.

PLoS Genet · 2012 · PMC3493449 · PMID 23144630

Europe PMCDOI
1
hedged sentence
0.0400
closest p · 0.8× alpha
0.0400
boldest claim

The sentences

moderately significantp = 0.04actually significant
Association between the C allele of rs4806718 with the affected status and the T allele with the asymptomatic status was moderately significant ( p = 0.04, by Fisher exact test).

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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.