Table 2. SNPs with genome-wide significant (p<5E-08) and suggestive (p<5E-07) results.

SNP	Chr	BP	EA	OA	EAF	nstu	n	β	SE	p	I2
rs10767094	11	3477509	A	G	0.48	6	8216	0.08	0.01	3E-09	47.6
rs12098951	11	3478953	A	G	0.48	8	10417	0.08	0.01	9E-09	52.3
rs10767093	11	3477421	T	A	0.48	8	10408	0.08	0.01	1E-08	40.3
rs10767096	11	3477891	T	C	0.53	8	10382	0.07	0.01	2E-08	47.6
rs202005905	11	54733705	I	D	0.84	9	15886	-0.08	0.01	4E-08	59.6
rs72854494	11	9946312	T	C	0.86	21	38330	-0.05	0.01	5E-08	0.0
rs188216744	14	106478354	T	C	0.55	5	7045	0.08	0.01	6E-08	87.2
rs115749482	16	16754648	A	G	0.81	5	6930	0.08	0.01	1E-07	85.6
rs59076561	11	9951438	G	T	0.86	20	35645	-0.05	0.01	1E-07	0.0
rs113227893	11	9944120	D	I	0.86	18	33850	-0.05	0.01	1E-07	0.2
rs67456791	11	9944108	G	A	0.86	20	35533	-0.05	0.01	1E-07	0.0
rs10767095	11	3477568	G	A	0.48	8	10413	0.07	0.01	2E-07	43.8
rs10834158	11	3477887	A	G	0.52	9	11682	0.07	0.01	2E-07	56.1
rs116657155	11	9954242	A	G	0.85	20	35619	-0.05	0.01	4E-07	0.0
rs60713856	11	9955418	G	C	0.85	20	35579	-0.05	0.01	4E-07	0.0
rs140557414	11	9953387	A	C	0.85	20	35632	-0.05	0.01	5E-07	0.0
rs57331333	11	9956272	T	C	0.85	20	35570	-0.05	0.01	6E-07	0.0
rs34543113	5	3339568	G	A	0.70	20	35612	-0.04	0.01	6E-07	0.0
rs11042555	11	9957159	T	C	0.85	20	35571	-0.05	0.01	7E-07	0.0
rs36189439	7	323206	A	G	0.58	6	7814	0.07	0.01	7E-07	69.2

Chr Chromosome

BP Basepair Position (Build 37 map)

EA Effect Allele

OA Other Allele

EAF Effect Allele Frequency

n_stu Number of Studies

n Sample Size

β Beta

SE standard error

p p-value

I² Effect heterogeneity