Table 3.

SNPs ^†present upstream and downstream of the two significant SNPs (rs3771150 and rs3771171)

CHR	SNP	CHR position	Alleles	Frequency in Cases	Frequency in Controls	p-value
2	rs974389	102303413	C/T	0.3235	0.3557	0.7116
2	rs12712141	102319499	C/T	0.5294	0.4375	0.2933
2	rs1041973	102321900	A/C	0.2812	0.5106	0.02247
2	rs1420101	102324148	A/G	0.5882	0.3814	0.02044
2	rs12712142	102327016	A/C	0.5588	0.3866	0.04901
2	rs1921622	102332499	A/G	0.5588	0.2526	0.000525
2	rs10208293	102332742	G/A	0.6176	0.4794	0.1404
2	rs4988955	102334360	A/G	0.5	0.2835	0.009945
2	rs4988956	102334439	G/A	0.5	0.2835	0.009945
2	rs10192036	102334643	C/A	0.5	0.2835	0.009945
2	rs10204137	102334644	A/G	0.5	0.2835	0.009945
2	rs10192157	102334788	C/T	0.5	0.2835	0.009945
2	rs10206753	102334794	T/C	0.5	0.2835	0.009945
2	rs13015714	102338297	G/T	0.05882	0.1094	0.3399
2	rs3755276	102344891	G/A	0.5882	0.3402	0.005714
2	§rs3771171	102352382	G/A	0.375	0.09278	5.75E-06
2	rs7579737	102353793	G/A	0.2353	0.3053	0.3804
2	rs2270297	102359107	A/G	0.1176	0.1031	0.786
2	rs7558013	102359238	T/G	0.1471	0.2577	0.1678
2	rs4851004	102375969	C/T	0.5625	0.2553	0.000791
2	rs2293225	102402321	T/C	0.2647	0.07216	0.000263
2	rs6743516	102402767	A/G	0.5588	0.2577	0.000635
2	rs13021177	102422925	A/G	0.6176	0.3802	0.003749
2	rs17027173	102423475	A/G	0.1471	0.2552	0.1681
2	§rs3771150	102427283	T/C	0.3824	0.09794	3.87E-06
2	rs11465730	102433290	A/G	0.3235	0.4639	0.126
2	rs11886793	102438652	G/T	0.2647	0.3802	0.1891

^†These are within 50kb upstream and downstream the two significant SNPs. Their chromosome (CHR) position, frequency in cases and controls, and p-values are shown;

^§The two significant SNPs are shown in bold; minor alleles are underlined.