Barely Significant
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Joint disease-specificity at the regulatory base-pair level.

Nat Commun · 2021 · PMC8260791 · PMID 34230488

Europe PMCDOI
1
hedged sentence
0.0050
closest p · 0.1× alpha
0.0050
boldest claim

The sentences

highly significantp < 0.005actually significant
In patients, the “A” allele frequency was 84.5%, a highly significant enrichment (e.g., 8.3% increase) compared to population controls at 76.2% ( p < 0.005).

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