Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation.

Nat Commun · 2016 · PMC4740744 · PMID 26831368

Europe PMC DOI

hedged sentence

0.0000

closest p · 0.0× alpha

0.0000

boldest claim

The sentences

highly significantP =3.34 × 10 −5actually significant

Nevertheless, the association of rs1363713 with AF trait was highly significant ( P =3.34 × 10 −5 ), but not as significant as the CNV.

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