Barely Significant
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Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events.

Circ Genom Precis Med · 2019 · PMC6625876 · PMID 30897348

2
hedged sentences
0.0400
closest p · 0.8× alpha
0.0400
boldest claim

The sentences

nominally significantP value = 0.04actually significant
We noted a borderline nominally significant interaction with sex, suggesting a greater risk among women with the chromosome 9p21 risk allele, for subsequent CHD death/MI (interaction P value = 0.04), whereas nonsignificant trends were noted for greater risk in those without hypertension ( P value=0.08) or without renal impairment ( P value=0.17).

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a marginal trendno p-value reported
However, there was no clear evidence of association for the remaining secondary outcomes, with only a marginal trend to protection for both subsequent heart failure (OR, 0.97; 95%, CI 0.93–1.01) and cardiovascular disease death (OR, 0.97; 95% CI, 0.94–1.01), as shown in Figure 2 .

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