Barely Significant
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Pathogenesis of premature coronary artery disease: Focus on risk factors and genetic variants.

Genes Dis · 2022 · PMC8843894 · PMID 35224153

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highly significantno p-value reported
65 A correlation between RECQL5 and cancer has been identified 64 ; however, it is unclear whether mutation of RECQL5 confers a highly significant risk of developing PCAD.

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