Genetic Variants at the 9p21.3 Locus Are Associated with Risk for Non-Compressible Artery Disease: Results from the ARTPER Study.

Genes (Basel) · 2023 · PMC10815029 · PMID 38275585

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marginally significantno p-value reported

At most, a marginally significant association was observed between an SNP in the 9p21.3 region and ABI values among individuals with NCAD and controls but only under a recessive genetic model, the one with the strongest association with NCAD.

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