Barely Significant
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<i>Complement C7</i> is a novel risk gene for Alzheimer's disease in Han Chinese.

Natl Sci Rev · 2019 · PMC6477931 · PMID 31032141

Europe PMCDOI
1
hedged sentence
0.0200
closest p · 0.4× alpha
0.0200
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The sentences

marginally significantP = 0.02actually significant
1C ), we recalculated the burden test excluding both rs3792646 and rs2271708, and observed a marginally significant enrichment of rare variants in cases ( P = 0.02), suggesting the existence of multiple effect alleles in C7 .

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