The impact of 22q11.2 copy-number variants on human traits in the general population.

Am J Hum Genet · 2023 · PMC9943723 · PMID 36706759

Europe PMC DOI

hedged sentence

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closest p · 1.0× alpha

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boldest claim

The sentences

nominally significantp < 0.05actually significant

For this purpose, nominally significant (p < 0.05) TWMR effects were retained and their direction was compared to the direction of the probe with the smallest nominally significant p value (p < 0.05) in the mirror association model for the corresponding gene ( ± 10 kb) and trait.

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