Barely Significant
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Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency.

Nat Genet · 2024 · PMC11387189 · PMID 39192094

Europe PMCDOI
1
hedged sentence
0.0170
closest p · 0.3× alpha
0.0170
boldest claim

The sentences

nominally significantP = 0.017actually significant
Under the additive model, the effect of p.(Arg162Ter) on twinning is nominally significant (OR = 1.46, P = 0.017), but does not meet our threshold for statistical significance after accounting for multiple testing (Supplementary Table 5 ).

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