Rare coding variants in CHRNB2 reduce the likelihood of smoking.

Nat Genet · 2023 · PMC10335934 · PMID 37308787

Europe PMC DOI

hedged sentence

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closest p · 0.0× alpha

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boldest claim

The sentences

moderately significantP = 1.1 × 10 −5actually significant

Additionally, the Arg460Gly variant independently showed a moderately significant protective association with the heavy smoker phenotype (OR = 0.56; CI = 0.43–0.72; P = 1.1 × 10 −5 ).

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