Table 4. Top results in the global meta-analysis.

CHR	Gene†	SNP	BP‡	A1	p	p(R)	OR	OR(R)	Q	I
9q31.1	LINC00587	rs1930551*	104380162	T	0.000117	0.008854	1.42	1.43	0.1005	56.48
9q31.1	LINC00587	rs10990158	104335927	T	0.000118	0.010900	1.41	1.42	0.0895	58.57
7q31.1	NRCAM	rs2041001*	107870335	G	0.000153	0.002704	1.46	1.46	0.1989	38.08
10q25.3	ABLIM1	rs941853	116189165	A	0.000196	0.009045	0.79	0.78	0.125	51.92
7p15.1	LOC402644	rs4722778	28278588	G	0.000253	0.025260	0.82	0.82	0.0617	64.11
12q21.33	LINC00615	rs10506984*	89217396	G	0.000347	0.000347	0.83	0.83	0.6274	0.00
9q31.1	LINC00587	rs7039568	104361604	T	0.000417	0.030730	1.37	1.40	0.0532	65.92
9q31.1	LINC00587	rs16921774*	104336206	T	0.000479	0.025540	1.36	1.38	0.0743	61.54
9q31.1	LINC00587	rs10990136	104298657	T	0.000831	0.039330	1.35	1.37	0.0581	64.85
5q21.1	ST8SIA4	rs2120913*	100096374	A	0.000852	0.000852	0.85	0.85	0.8767	0.00
9q31.1	LINC00587	rs7024470	104361506	G	0.000941	0.030740	1.34	1.36	0.0777	60.87

CHR: Chromosome; BP: Base pair position; SNP: Single Nucleotide Polymorphism; A1: Reference allele (minor allele); p: Fixed-effects p-value; p(R): Random-effects p-value; OR: Fixed-effects Odds Ratio; OR(R): Random-effects Odds Ratio; Q: p-value for heterogeneity of OR; I: effect size for heterogeneity of OR.

*SNPs selected by two-locus association analyses in the NXC-GWAS sample.

^†The nearest gene or the gene where the SNP is located.

^‡According to UCSC genome browser (NCBI36/hg18) and dbSNP build 130.