Characterising heart rhythm abnormalities associated with Xp22.31 deletion.

J Med Genet · 2023 · PMC10359567 · PMID 36379544

Europe PMC DOI

hedged sentence

0.0410

closest p · 0.8× alpha

0.0410

boldest claim

The sentences

nominally significantp=0.041actually significant

26 Gene-based analysis suggested a nominally significant association between STS (chrX:7 065 298–7 272 682, GRCh37/h19 genome build) and AF in males (4556 cases (2.7%) vs 163 499 controls (97.3%), p=0.041) but not in females (2144 cases (1.1%) vs 193 494 controls (98.9%), p=0.793) ( table 1 and figure 2 ).

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