Table 2.

Basic information of candidate SNPs

SNP ID	Gene Name	Allele (A/B)	Chromosome position	MAF		HWE p	ORs	95% CI		p
				Case	Control
rs11249433	LOC647121	C/T	chr1: 121280613	0.019	0.033	0.892	0.57	0.23	1.46	0.238
rs2981579	FGFR2	C/T	chr10: 123337335	0.431	0.480	0.706	0.82	0.62	1.10	0.180
rs1219648	FGFR2	G/A	chr10: 123346190	0.494	0.452	0.998	1.19	0.89	1.58	0.139
rs10510102	ATE1	G/A	chr10: 123625190	0.157	0.206	0.766	0.72	0.49	1.04	0.081
rs2380205		T/C	chr10: 5886734	0.144	0.086	0.915	1.79	1.13	2.83	0.012*
rs10822013	ZNF365	T/C	chr10: 64251977	0.489	0.447	0.888	1.19	0.89	1.58	0.245
rs10995190	ZNF365	A/G	chr10: 64278682	0.022	0.005	0.997	4.40	0.93	20.88	0.086
rs704010	ZMIZ1	A/G	chr10: 80841148	0.343	0.302	0.010#	1.21	0.89	1.64	0.223
rs3817198	LSP1	C/T	chr11: 1909006	0.119	0.145	0.474	0.80	0.52	1.22	0.294
rs614367		T/C	chr11: 69328764	0.019	0.005	0.997	3.86	0.80	18.73	0.071
rs999737	RAD51L1	T/C	chr14: 69034682	0.003	0.005	0.997	0.54	0.05	5.98	0.610
rs3803662	TOX3	C/T	chr16: 52586341	0.315	0.334	0.795	0.92	0.67	1.24	0.573
rs3112612	LOC643714	C/T	chr16: 52635164	0.255	0.216	0.997	1.25	0.89	1.75	0.197
rs4973768	SLC4A7	T/C	chr3: 27416013	0.261	0.234	0.882	1.16	0.83	1.61	0.380

^#site with HWE p ≤ 0.01 is excluded;

^* p value ≤ 0.05 indicates statistical significance;

Abbreviations: SNP, single nucleotide polymorphism; MAF, minor allele frequency; HWE, Hardy-Weinberg equilibrium; OR, odd ratio; CI, confidence interval; A/B stands for minor/major alleles on the control sample frequencies.