Barely Significant
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ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease.

PLoS Genet · 2021 · PMC8109807 · PMID 33909604

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

The sentences

nominally significantP < 0.05actually significant
Lack of statistical power was also a challenge in our study: in the FinnGen data, the association between the Finnish-enriched ANGPTL8 PTV was nominally significant ( P < 0.05) but not after multiple-testing correction.

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