WDR35 and coronary artery disorder: To further explore the associations between polymorphism in the locus and CAD risk and to facilitate the determination of genuinely associated variants and the establishment of complete molecular pathways underlying the pathogenesis of CAD, we conducted a CAD case‐control study in Han Chinese to test five SNPs (rs12617744, rs2278528, rs7594214, and rs3731661, rs721932) in TTC32‐WDR35 gene cluster.