Table 1. Summary results for the tested SNPs in 252 patients with unexplained adenomatous polyposis and 745 healthy controls.

			Allele*		MAF
Chr	SNP	Base-pair position†	Minor	Major	Patients	Controls	p Value	OR (95% CI)	Gene	Reference
1q41	rs6691170	222045446	T	G	0.378	0.346	0.194	1.1 (0.9-1.4)	DUSP10 CICP13	32
1q41	rs6687758	222164948	G	A	0.228	0.197	0.141	1.2 (0.9 to 1.5)	DUSP10 CICP14	32
3q26.2	rs10936599	169492101	T	C	0.237	0.244	0.745	1.0 (0.8 to 1.2)	MYNN	32
8q23.3	rs16892766	117630683	C	A	0.086	0.086	0.998	1.0 (0.7 to 1.4)	TRPS1 EIF3H	33
8q24.21	rs6983267	128413305	G	T	0.575	0.530	0.078	1.2 (1.0 to 1.5)	POU5F1 MYC	34
10p14	rs10795668	8701219	A	G	0.290	0.324	0.154	0.9 (0.7 to 1.1)	KRT8P16 TCEB1P3	33
11q23	rs3802842	111171709	C	A	0.355	0.256	0.00002	1.6 (1.3 to 2.0)	C11orf93	11
12q13.13	rs7136702	50880216	T	C	0.357	0.327	0.222	1.1 (0.9 to 1.4)	TBX3 UBA52P7	32
12q13.13	rs11169552	51155663	T	C	0.260	0.264	0.876	1.0 (0.8 to 1.2)	DIP2B ATF1	32
14q22.2	rs4444235	54410919	C	T	0.444	0.437	0.763	1.0 (0.8 to 1.3)	RPS3AP46 BMP4	12
15q13	rs4779584	32994756	T	C	0.256	0.187	0.001	1.5 (1.2 to 1.9)	SCG5 GREM1 FMN1 CRAC1	35
16q22.1	rs9929218	68820946	A	G	0.280	0.278	0.921	1.0 (0.8 to 1.3)	CDH1	12
18q21.1	rs4939827	46453463	C	T	0.486	0.491	0.864	1.0 (0.8 to 1.2)	SMAD7	14
19q13.1	rs10411210	33532300	T	C	0.090	0.092	0.918	1.0 (0.7 to 1.4)	RHPN2	12
20p12.3	rs961253	6404281	A	C	0.386	0.375	0.661	1.0 (0.9 to 1.3)	TARDBPL BMP2	12
20q13.33	rs4925386	60921044	T	C	0.297	0.316	0.423	0.9 (0.7 to 1.1)	LAMA5	32

^*For SNP rs6983267, the minor allele originally reported (G) is the most frequent allele, both in our cases and controls.

^†The SNP positions are according to Human Build 36.3.

Chr, chromosome; MAF, minor allele frequency.