Barely Significant
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Health improvements by understanding residual risk in coronary artery disease and new targets for prevention/treatment: rationale and research protocol of the HURRICANE project.

Eur Heart J Open · 2025 · PMC11823827 · PMID 39949422

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highly significantno p-value reported
Genetic variants with a highly significant risk loci (high frequency typically above 5%) and their association with clinical patterns of cardiometabolic/vascular risk and CAD endpoints will be exploited by discovery platform collecting variants associated to human diseases (e.g.

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