Study of variants in genes implicated in rare familial migraine syndromes and their association with migraine in 200,000 exome-sequenced UK Biobank participants.

Ann Hum Genet · 2022 · PMC9804876 · PMID 36044383

Europe PMC DOI

hedged sentence

0.0400

closest p · 0.8× alpha

0.0400

boldest claim

The sentences

nominally significantp = 0.04actually significant

The p.(Glu492Lys) variant in ATP1A2 occurs in 18 cases versus 298 controls, a result which is nominally significant at p = 0.04, but again this is not statistically significant after correction for multiple testing.

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