Barely Significant
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Contribution of copy number variations to the risk of severe eating disorders.

Psychiatry Clin Neurosci · 2022 · PMC9546291 · PMID 35611833

Europe PMCDOI
1
hedged sentence
0.0254
closest p · 0.5× alpha
0.0254
boldest claim

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nominally significantP = 0.0254actually significant
In gene set analysis, we observed a nominally significant enrichment of rare exonic CNVs in synaptic signaling in ED patients (odds ratio = 2.55, P = 0.0254).

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