CYP4V2 rs56413992 C > T was associated with the risk of coronary heart disease in the Chinese Han population: a case–control study

Table 2 Basic information and allele frequency distribution of CYP4V2 SNPs

SNP_ID	Gene	Chr: Position	Consequence	Allele	MAF		HWE p-value	OR (95% CI)	p
SNP_ID	Gene	Chr: Position	Consequence	Allele	Case	Control	HWE p-value	OR (95% CI)	p
rs1398007	CYP4V2	4: 186,191,678	5'-UTR	C > T	0.324	0.294	0.585	1.16(0.95–1.40)	0.141
rs13146272	CYP4V2	4: 186,199,057	Missense	C > A	0.390	0.383	0.632	1.03(0.86–1.24)	0.753
rs3736455	CYP4V2	4: 186,201,165	Synonymous	T > G	0.394	0.394	0.448	1.00(0.84–1.20)	0.984
rs1053094	CYP4V2	4: 186,211,877	3'-UTR	T > A	0.367	0.338	0.480	1.13(0.94–1.36)	0.195
rs56413992	CYP4V2	4: 186,213,040	3'-UTR	C > T	0.229	0.179	1.000	1.36(1.09–1.70)	0.007

SNP single nucleotide polymorphism, Chr Chromosome, MAF minor allele frequency, HWE Hardy–Weinberg equilibrium, OR odds ratio, 95% CI 95% confidence interval
Bold values indicated that the p-value was statistically significant
p-value was calculated with Person’s chi-square test

ISSN: 1755-8794