Barely Significant
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The rs34416841 polymorphism in the Alu element of the circSirt1 flanking intron is associated with an increased risk of myocardial infarction.

BMC Med Genomics · 2025 · PMC12797537 · PMID 41353146

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borderline significanceno p-value reported
These findings highlight two critical considerations: (1) rigorous multiple testing correction is essential in genetic epidemiology to mitigate false-positive results from extensive subgroup analyses; and (2) observed subgroup associations, particularly those with borderline significance, should be interpreted as hypothesis-generating rather than definitive evidence.

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