Barely Significant
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Polygenic basis and biomedical consequences of telomere length variation.

Nat Genet · 2021 · PMC8492471 · PMID 34611362

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

The sentences

nominally significantP < 0.05actually significant
For an additional 12 traits, we found nominally significant associations ( P < 0.05) with genetically determined LTL, with most of these traits showing significant and concordant associations with usual LTL (Fig. 4 and Supplementary Table 10 ).

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