A phenome-wide scan reveals convergence of common and rare variant associations.

Genome Med · 2023 · PMC10683189 · PMID 38017547

Europe PMC DOI

hedged sentence

0.0500

closest p · 1.0× alpha

0.0500

boldest claim

The sentences

nominally significantP < 0.05actually significant

We included 412 heritable traits with nominally significant p -value ( P < 0.05) from the common variant-based h 2 estimation (as implemented in ldsc) in the downstream analyses.

also in 7,732 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.