Barely Significant
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Genotype-Phenotype Association for 14 <i>GFAP</i> Variants in Alexander Disease.

Neurol Genet · 2025 · PMC12166557 · PMID 40520824

Europe PMCDOI
1
hedged sentence
0.0580
closest p · 1.2× alpha
0.0580
boldest claim

The sentences

failed to achieve significancep = 0.058so close (0.05 < p ≤ 0.1)
p = 1.000] clearly failed to achieve significance, the differences between R258C and N77S [adj. p = 0.058] and between R70W and N77S [adj. p = 0.055] being slightly above the significance threshold.

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