Barely Significant
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Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients.

TH Open · 2018 · PMC6524857 · PMID 31249928

Europe PMCDOI
1
hedged sentence
0.0300
closest p · 0.6× alpha
0.0300
boldest claim

The sentences

nominally significantp = 0.03actually significant
Only one SNV showed a nominally significant allele frequency difference (rs6489695, p = 0.03).

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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.