Barely Significant
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Prion protein codon 129 polymorphism in mild cognitive impairment and dementia: the Rotterdam Study.

Brain Commun · 2020 · PMC7425338 · PMID 32954288

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

The sentences

borderline significantP = 0.08so close (0.05 < p ≤ 0.1)
Carriers of the VV genotype showed a borderline significant higher prevalence of mild cognitive impairment than heterozygous carriers (odds ratio, 1.37; 95% confidence interval, 0.96–1.97; P = 0.08).

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