Barely Significant
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Systematic prioritization of functional variants and effector genes underlying colorectal cancer risk.

Nat Genet · 2024 · PMC11525171 · PMID 39284974

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hedged sentence
closest p
boldest claim

The sentences

highly significantno p-value reported
As this might not capture functional variants that remain highly significant at some loci (that is, where the lead variant has an extremely strong association), we also considered variants having −log 10 ( P variant ) > 0.7 × (−log 10 ( P lead variant )), stipulating an r 2 of >0.2 for the lead variant and a P variant of <10 −5 in the GWAS.

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