Barely Significant
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9p21.3 coronary artery disease risk locus and interferon alpha 21: Association study in an Asian Indian population.

Indian Heart J · 2019 · PMC7136328 · PMID 32248921

2
hedged sentences
0.0610
closest p · 1.2× alpha
0.0640
boldest claim

The sentences

showed a trendp = 0.061so close (0.05 < p ≤ 0.1)
SNPstat analysis revealed that the TT and TC genotypes of rs10757272 showed a significant risk association among female CAD patients (OR = 8.15 for TC and 9.27 for TT, p = 0.012 in the codominant model), CC genotype of rs1333045 showed a significant risk association among all CAD patients (OR = 1.46, p = 0.046 in the recessive model), CC genotype of rs1333049 showed a trend toward risk association among premature (age at presentation < 55 years in males and <65 years in females) CAD patients (OR = 1.61, p = 0.061 in the recessive model), and GG genotype of rs4977574 showed a significant risk association among premature CAD patients (OR = 1.77, p = 0.025 in the recessive model).

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approaching significancep = 0.064so close (0.05 < p ≤ 0.1)
• Age: Among controls, there is a higher proportion of individuals in the high-level IFNA21 group in both the age categories (<50 years and ≥50 years), with the p -value approaching significance ( p = 0.064).

also in 2,640 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.