Barely Significant
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Genomic and ancestral variations linked to the development of post-acute sequelae of SARS-CoV-2 infection in Indian populations.

Front Genet · 2025 · PMC12815448 · PMID 41561974

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0.0001
closest p · 0.0× alpha
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boldest claim

The sentences

highly significantp < 0.0001actually significant
SNVs showing highly significant association ( p < 0.0001) mapped to pathways related to neuronal signaling, axon guidance, neural cell adhesion molecule interactions and acetylation, extracellular matrix (ECM) organization, olfactory signaling, Rho-GTPase cycle, and G- α signaling events ( Supplementary Figure S1 ).

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