Table 1.

Genome-wide association results for genetic variants with an association p-value < 5 × 10⁻⁶.

SNP	Chr	BPa	EAb	NEAb	EAFb	Beta	SE	P	Directionc	HetPVald	N	RefGene
rs7114256	11	78539553	A	G	0.92	0.129	0.03	8.78E-07	+++++−?++	0.74	13,003	ODZ4
rs606243	2	4487817	A	G	0.74	−0.078	0.02	1.42E-06	------??-	0.36	11,862	ALLC
rs17496593	5	104254353	A	C	0.91	−0.111	0.02	2.12E-06	-----+?--	0.21	13,005	NUDT12
rs17496653	5	104255187	A	G	0.09	0.110	0.02	2.58E-06	+++++−?++	0.20	13,005	NUDT12
rs17562893	5	104266799	T	G	0.09	0.108	0.02	3.78E-06	+++++−?++	0.19	12,994	NUDT12
rs7103693	11	78535307	T	C	0.08	−0.120	0.03	4.19E-06	-----+?--	0.79	13,003	ODZ4

^aPhysical Position (base pair) in build 36.

^bEA: effect allele, NEA: non-effect allele, EAF: effect allele frequency.

^cThe sign of EA effect and the order of Cohorts are BHS, COLAUS, DESIR, ERGO, FHS, HBCS, KORA, PREVEND, SARDIANA.

^dHetPVal: P-value for testing for heterogeneity.

^eRefGen: closest reference gene.