Barely Significant
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Questioning the Association of the <i>STMN2</i> Dinucleotide Repeat With Amyotrophic Lateral Sclerosis.

Neurol Genet · 2022 · PMC9342143 · PMID 35923349

Europe PMCDOI
1
hedged sentence
0.0410
closest p · 0.8× alpha
0.0410
boldest claim

The sentences

nominally significantp = 0.041actually significant
Although there was a nominally significant p value of L/L with 24CA using the CMH test combining allele counts from the current cohort and the Australian cohort from the previous study ( p = 0.041), this result does not pass the multiple testing correction threshold (α = 0.05/10; p = 0.005).

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