Other variants associated with coronary artery disease included a missense variant (p.Gly567Arg; AF = 0.9%, OR = 2.0, P = 5.2 × 10−12) in HHIPL1, which was associated with coronary revascularization (n = 12,271), and a splice acceptor variant (c.7325-2A>G; AF = 0.7%, OR = 2.5, P = 2.9 × 10−08) in NBEAL1, which was associated with coronary artery bypass grafting (n = 5,779). Here, HHIPL1 is linked to atrial fibrillation.