Barely Significant
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De novo missense variants in FBXO11 alter its protein expression and subcellular localization.

Hum Mol Genet · 2022 · PMC8825234 · PMID 34505148

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0.0130
closest p · 0.3× alpha
0.0130
boldest claim

The sentences

nominally significantP = 0.013actually significant
Overweight/hyperphagia were more common in individuals carrying LGD variants compared to carriers of missense variants with a nominally significant P -value [ Table 1 , chi-square test, 46% versus 18% ( P = 0.013)].

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