Barely Significant
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Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia.

Mol Psychiatry · 2018 · PMC5984079 · PMID 28630456

Europe PMCDOI
1
hedged sentence
0.0061
closest p · 0.1× alpha
0.0061
boldest claim

The sentences

nominally significantP =0.0061actually significant
Unlike singleton disruptive variants, although the burden of rare disruptive variants in SCZ was nominally significant, and survived FWER correction for all tests within the trait, it did not meet the threshold for tests across all traits (unadjusted P =0.0061, FWER within P =0.0228, FWER across P =0.0863, Supplementary Table S9 ).

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