Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders.

Genet Med · 2021 · PMC8257493 · PMID 33731876

Europe PMC DOI

hedged sentence

0.0100

closest p · 0.2× alpha

0.0100

boldest claim

The sentences

nominally significantp = 0.01actually significant

Phenotypic similarity analysis for locations within the NaV1.2 channel and recurrent variants Phenotypic similarity was nominally significant between individuals with missense variants regardless of location ( p = 0.01, n = 341) and also among individuals with missense variants localized to either the S1 segment ( p = 0.009, n = 18) or domain DIV ( p = 0.05, n = 65).

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.