Barely Significant
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Genotype-phenotype correlations in patients with de novo <i>KCNQ2</i> pathogenic variants.

Neurol Genet · 2020 · PMC7803337 · PMID 33659638

1
hedged sentence
0.0800
closest p · 1.6× alpha
0.0800
boldest claim

The sentences

a trend toward significancep = 0.08so close (0.05 < p ≤ 0.1)
Both models (table e-3, links.lww.com/NXG/A334 ) failed to show a correlation between localization of the variants (TM vs others) and patients' cognitive outcome (normal/abnormal), whereas analysis of time to seizure offset (≤1 year/>1 year) showed a trend toward significance for model 2 ( p = 0.08 ).

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