Barely Significant
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Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program.

Front Genet · 2023 · PMC10755672 · PMID 38162683

Europe PMCDOI
1
hedged sentence
0.0052
closest p · 0.1× alpha
0.0052
boldest claim

The sentences

marginally significantp = 5.15E-03actually significant
While not statistically significantly associated with aTRH in our other analyses, the variant had a consistent direction of effect in all our analyses, with marginally significant p -values for the multi-ethnic aTRH versus treated controls (OR [95% CI] = 0.88 [0.80–0.96], p = 5.15E-03), AA aTRH versus normotensive controls (OR [95% CI] = 0.83 [0.72–0.95], p = 8.47E-03), and EA aTRH versus normotensive controls (OR [95% CI] = 0.81 [0.69–0.94], p = 5.81E-03).

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