Barely Significant
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Variants of the CASP9 gene as candidate markers for primary response to anti-TNF therapy in Crohn's disease patients.

J Appl Genet · 2023 · PMC10632275 · PMID 37658984

1
hedged sentence
0.0700
closest p · 1.4× alpha
0.0700
boldest claim

The sentences

near statistical significancep = 0.07so close (0.05 < p ≤ 0.1)
The results for the third variant rs4645978 are near statistical significance ( p = 0.07).

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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.