Table 2. Allele frequencies in cases and controls and odds ratio estimates for CHD.

SNP ID	Gene(s)	Band	Alleles Aa/B	MAF		HWEp	ORs	95% CI	p
				Case	Control
Male
rs11206831	PPAP2B	1p32.2	T/C	0.050	0.055	1	0.909	0.559-1.478	0.700
rs1759752	PPAP2B	1p32.2	C/G	0.220	0.168	0.8558	1.401	1.066-1.841	0.015*
rs1930760	PPAP2B	1p32.2	T/C	0.490	0.467	0.4733	1.093	0.881-1.356	0.418
rs12566304	PPAP2B	1p32.2	A/C	0.132	0.148	0.1561	0.877	0.643-1.198	0.410
rs914830	PPAP2B	1p32.2	T/C	0.324	0.329	0.8172	0.976	0.776-1.229	0.838
Female
rs11206831	PPAP2B	1p32.2	T/C	0.050	0.045	1	1.011	0.530-1.928	0.975
rs1759752	PPAP2B	1p32.2	C/G	0.209	0.165	1	1.338	0.950-1.883	0.094
rs1930760	PPAP2B	1p32.2	T/C	0.442	0.498	0.7299	0.799	0.610-1.046	0.102
rs12566304	PPAP2B	1p32.2	A/C	0.161	0.148	0.1653	1.099	0.759-1.591	0.619
rs914830	PPAP2B	1p32.2	T/C	0.339	0.348	0.1621	0.961	0.724-1.246	0.784

MAF, minor allelic frequency; HWE, Hardy-Weinberg Equilibrium; ORs, odds ratios; CI: confidence interval.

^a Minor allele; *p ≤ 0.05 indicates statistical significance;