Table 2. Relation of single nucleotide polymorphisms (SNPs) to coronary artery disease as determined by multivariable logistic regression analysis.

SNP		Dominant		Recessive		Additive 1		Additive 2
		P	OR (95% CI)	P	OR (95% CI)	P	OR (95% CI)	P	OR (95% CI)
rs58098972	A/G	0.0064	1.16 (1.04–1.29)	0.2601		0.0118	1.15 (1.03–1.29)	0.1780
rs77336780	C/G (A304G)	0.0355	0.90 (0.81–0.99)	0.0145	0.74 (0.57–0.94)	0.1381		0.0085	0.72 (0.55–0.92)
rs200121865	G/C (G149A)	0.0034	2.27 (1.32–3.86)	0.0682		0.0065	2.16 (1.25–3.69)	0.0679
rs202069030	G/C (R51S)	0.0099	0.32 (0.09–0.78)	ND		0.0099	0.32 (0.09–0.78)	ND
rs7188	T/G	0.5784		0.0009	0.76 (0.64–0.89)	0.6171		0.0025	0.77 (0.65–0.91)
rs2271395	A/G (T1587A)	0.0023	0.85 (0.77–0.94)	0.0918		0.0084	0.86 (0.77–0.96)	0.0052	0.82 (0.72–0.94)

Multivariable logistic regression analysis was performed with adjustment for age, sex, and the prevalence of hypertension, diabetes mellitus, and dyslipidemia. Based on Bonferroni's correction, a P value of <9.92 × 10⁻⁵ (0.05/504) was considered statistically significant. OR, odds ratio; CI, confidence interval; ND, not determined.