Table 1.

Genetic variants with the lowest P values

SNP	Chr	Position	MAF	Gene	Common allele	Minor allele	Type	Odds ratio (95% CI)	P value
rs4784750	16	57056064	0.273	NLRC5	G	T	I	1.38 (1.23–1.54)	1.56E-8
rs16972207	13	108929066	0.185	TNFSF13B	C	G	I	1.54 (1.32–1.79)	3.42E-8
rs17564816	13	108927503	0.185	TNFSF13B	G	A	I	1.52 (1.31–1.77)	4.01E-8
rs4784751	16	57056574	0.270	NLRC5	C	T	O	1.36 (1.22–1.52)	4.07E-8
rs12444396	16	57057194	0.264	NLRC5	G	A	I	1.36 (1.21–1.52)	8.43E-8
rs12445252	16	57057679	0.264	NLRC5	C	T	I	1.36 (1.21–1.52)	8.90E-8
rs61972007	13	108918701	0.191	TNFSF13B	A	G	I	1.42 (1.25–1.62)	1.37E-7
rs61971976	13	108889127	0.216	TNFSF13B	G	A	I	1.39 (1.23–1.58)	1.60E-7
rs61971980	13	108899416	0.186	TNFSF13B	G	A	I	1.40 (1.23–1.60)	1.87E-7
rs3900097	13	108905819	0.186	TNFSF13B	C	T	I	1.40 (1.23–1.60)	1.88E-7

Abbreviations: Chr, chromosome; I, imputed single nucleotide polymorphism; MAF, minor allele frequency; O, originally genotyped single nucleotide polymorphism.