Barely Significant
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Genetic variation in NFE2L2 is associated with outcome following aneurysmal subarachnoid haemorrhage.

Eur J Neurol · 2023 · PMC10092511 · PMID 36148820

Europe PMCDOI
1
hedged sentence
0.0050
closest p · 0.1× alpha
0.0050
boldest claim

The sentences

highly significantp = 0.005actually significant
A fixed‐effects meta‐analysis of rs10183914 in the discovery and validation cohorts identified a highly significant estimated OR of 1.34 (95% CI 1.09–1.64; p = 0.005).

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