. Author manuscript; available in PMC: 2014 Jul 1.

Published in final edited form as: Hum Genet. 2013 Mar 31;132(7):803–810. doi: 10.1007/s00439-013-1292-5

Table 1. Odds ratios (ORs) and 95 % confidence intervals (CIs) of the rs4424066 and rs3817963 SNPs in the BTNL2 gene.

SNP^a	Risk allele frequency (%)		Individual models^b				Combined model^e

	Cases (n = 486)	Controls (n = 943)	Heterozygous OR (95 % CI)^f	Homozygous OR (95 % CI)^f	Per allele OR (95 % CI)^f	p for trend	Per allele OR (95 % CI)^f	p for trend
Individual models^b
rs4424066 (A/G)^c	70.6	66.0	1.20 (0.81–1.77)	1.49 (1.02–2.19)	1.23 (1.04–1.45)	0.015	1.05 (0.85–1.30)	0.65
rs3817963 (A/G)^d	86.9	82.1	4.63 (1.39–15.4)	5.95 (1.81–19.6)	1.46 (1.16–1.82)	0.001	1.40 (1.06–1.86)	0.02

Risk allele/reference allele

ORs were estimated for each SNP in individual models

Perfect proxy of rs2076530 in Hapmap YRI

Perfect proxy of rs9268480 in Hapmap YRI

ORs were estimated in a single combined model that contained both SNPs

Adjusted for % of African ancestry, age, and region of residence