Barely Significant
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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.

Nat Genet · 2016 · PMC4986048 · PMID 26998691

Europe PMCDOI
1
hedged sentence
0.0500
closest p · 1.0× alpha
0.0500
boldest claim

The sentences

nominally significantp=0.05actually significant
The strength of the association between LoF+DCM burden and case status (at p=7.6e-15 without controlling for Vineland scores), is only nominally significant after Vineland score is controlled for (p=0.05).

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