Barely Significant
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RNF213 Variants, Vasospastic Angina, and Risk of Fatal Myocardial Infarction.

JAMA Cardiol · 2024 · PMC11195602 · PMID 38888930

1
hedged sentence
0.1700
closest p · 3.4× alpha
0.1700
boldest claim

The sentences

showed a trendP = .17not close (p > 0.1)
Moreover, the haplotype analysis demonstrated that the risk allele of rs111321460 was consistently present in the same haplotype as the risk allele of rs112735431 and that the low-frequency haplotype containing the risk variant of rs112735431 and the reference allele of rs111321460 still showed a trend of association (OR, 1.40; 95% CI, 0.83-2.23; P = .17) (eTable 4 in Supplement 1 ).

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