Table 1. Case-control association for genotyped variants in AA and EA.

SNP	Position	Alleles	AA				EA
			Affected	Control	P-value	OR	Affected	Control	P-value	OR
			(N = 1525)	(N = 4485)		[95%CI]	(N = 3968)	(N = 9750)		[95%CI]
rs13023380	162,862,609	G/A	0.885	0.911	4.33×10−5 +	0.75	0.433	0.478	9.52×10−11 +	0.84
					3.92×10−4 *	(0.66–0.86)			6.66×10−11 *	(0.79–0.88)
					1.75×10−2 **				8.71×10−11 **
rs10930046	162,846,229	G/A	0.374	0.428	1.81×10−7 +	0.80	0.016	0.013	8.61×10−2 +	1.21
					3.22×10−6 *	(0.73–0.87)			8.4×10−2 *	(0.97–1.50)
					8.51×10−6 **				0.12**
rs1990760	162,832,297	G/A	0.799	0.829	2.02×10−4 +	0.82	0.375	0.400	1.22×10−4 +	0.90
					2.61×10−3 *	(0.74–0.91)			1.44×10−4 *	(0.85–0.95)
					1.43×10−2 **				1.74×10−4 **

The numbers of affected and control samples are provided in parentheses. Allele frequencies, odds ratios (OR), and 95% confidence intervals [95% CI] are given for the ‘G’ alleles. Allelic association legends are:

⁺uncorrected;

^*corrected by local ancestry; and

^**corrected by global ancestry.