Barely Significant
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<i>GNE</i> genotype explains 20% of phenotypic variability in GNE myopathy.

Neurol Genet · 2019 · PMC6384023 · PMID 30842975

Europe PMCDOI
1
hedged sentence
0.0100
closest p · 0.2× alpha
0.0100
boldest claim

The sentences

only marginally significantp > 0.01actually significant
In a multivariate model using all variables homozygosity was only marginally significant ( p > 0.01).

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