Barely Significant
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A Genetic Risk Prediction Model for Coronary Artery Disease Integrating CYP17A1 Polymorphisms and Clinical Variables in a Chinese Population.

Int J Gen Med · 2026 · PMC12960047 · PMID 41798299

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nominally significantno p-value reported
Additionally, the dominant model (TT vs CC + CT) of rs4409766 showed a nominally significant difference, suggesting the TT genotype could increase the susceptibility to CAD in males.

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