Table 1.

Single locus analysis for all the single nucleotide polymorphisms (SNPs) genotyped in NLGN3 and NLGN4X (EUR control population).

Gene ID	SNP ID	Minor Allele	MAF Controls	MAF Case	p-Value	OR	95% CI	p-Corr
NLGN3	rs11795613	G	0.481	0.515	0.398	1.144	0.816–1.617	0.701
	rs4844285	A	0.4741	0.4895	0.701	1.064	0.755–1.496	0.701
	rs4844286	T	0.505	0.481	0.5396	0.908	0.646–1.280	0.701
NLGN4X	rs6638575	A	0.266	0.301	0.303	1.193	0.856–1.663	0.404
	rs3810688	T	0.2176	0.288	0.0456	1.453	1.018–2.074	0.152
	rs3810687	T	0.1086	0.1339	0.3369	1.269	0.805–2.000	0.404
	rs3810686	T	0.4466	0.4561	0.817	1.039	0.768–1.407	0.817
	rs5916269	A	0.1086	0.1339	0.3369	1.269	0.805–2.000	0.404
	rs1882260	C	0.2655	0.3347	0.0505	1.392	1.005–1.928	0.152

Statistical significance, for the single locus association analysis, was tested at p < 0.05, after Fisher’s exact test. The p-values have been adjusted by false discovery rate (FDR) correction for multiple test analysis. MAF controls, frequency of the minor allele in controls (n = 379); MAF case, frequency of the minor allele in case (n = 202); OR, odds ratio; CI, confidence interval; p-corr, corrected p-value after FDR test.