Table 4.

SNPs Associated with Antisaccade Error Rate with p Values Less than 10⁻⁴

SNP	Chr	Position	Allele1	Alelle2	Beta	SE	t	p	Gene	Class
rs4973397	2	232291471	G	A	0.031	0.006	5.425	6.10E-08
rs12998237	2	232276651	G	A	0.031	0.006	5.405	6.83E-08
rs2290130	2	232263127	A	G	0.029	0.006	5.114	3.28E-07	B3GNT7	multiple
rs13030174	2	232271284	C	A	0.028	0.006	4.867	1.17E-06
rs1868455	2	232278400	G	A	0.023	0.005	4.597	4.40E-06
rs13240504	7	126089319	A	G	0.032	0.007	4.568	5.06E-06	GRM8	intron
rs1840108	2	181366251	A	C	0.040	0.009	4.544	5.66E-06
rs2028162	11	16247475	G	A	−0.025	0.006	−4.526	6.17E-06	SOX6	intron
rs13235082	7	126099842	A	C	0.032	0.007	4.493	7.20E-06	GRM8	intron
rs763564	12	91024916	A	G	0.031	0.007	4.438	9.29E-06
rs3857348	5	10297847	A	G	−0.022	0.005	−4.371	1.27E-05	CMBL	intron
rs4621162	2	232284911	G	A	0.022	0.005	4.361	1.32E-05
rs4368910	7	98439700	A	G	−0.022	0.005	−4.319	1.60E-05
rs2520497	12	91022310	G	A	0.033	0.008	4.303	1.72E-05
rs1913754	10	82423687	G	A	0.023	0.005	4.261	2.07E-05
rs9310429	3	13711684	G	A	0.033	0.008	4.247	2.21E-05	LINC00620	intron
rs11135869	8	25335354	G	A	0.022	0.005	4.196	2.77E-05	CDCA2	intron
rs583297	6	153349813	G	A	−0.021	0.005	−4.196	2.77E-05	RGS17	intron
rs10254771	7	125960953	A	G	0.029	0.007	4.134	3.64E-05
rs7136250	12	131417075	G	A	−0.021	0.005	−4.121	3.84E-05
rs6901674	6	78946797	A	G	0.110	0.027	4.110	4.03E-05
rs12907899	15	34151519	G	A	0.020	0.005	4.091	4.37E-05	RYR3	intron
rs6074043	20	44781380	A	G	0.024	0.006	4.090	4.40E-05
rs9644041	8	25321281	G	A	0.021	0.005	4.087	4.45E-05	CDCA2	intron
rs1836789	19	56489456	G	A	−0.022	0.005	−4.084	4.50E-05	NLRP8	intron
rs1422812	5	169069114	G	A	0.027	0.007	4.077	4.64E-05	DOCK2	intron
rs2369271	2	232289244	G	A	0.022	0.005	4.066	4.86E-05
rs4770248	13	22794240	A	G	0.022	0.005	4.049	5.23E-05	LINC00540	intron
rs1061375	3	13679203	A	G	0.022	0.005	4.038	5.49E-05	FBLN2	synon codon
rs4236538	7	98434486	A	G	−0.020	0.005	−4.033	5.60E-05
rs701265	3	152554357	G	A	0.028	0.007	4.011	6.14E-05	P2RY1	synon codon
rs6786253	3	152575924	G	A	0.028	0.007	4.003	6.37E-05
rs2903455	4	79095407	G	A	0.028	0.007	4.001	6.42E-05	FRAS1	intron
rs6440825	3	152572930	G	A	0.028	0.007	3.995	6.57E-05
rs1415707	13	98496595	A	G	−0.020	0.005	−3.993	6.64E-05
rs6733349	2	232268312	G	A	0.021	0.005	3.979	7.02E-05
rs2180477	20	14759169	A	G	0.051	0.013	3.967	7.38E-05	MACROD2	intron
rs1776438	6	37553497	A	G	0.023	0.006	3.963	7.52E-05
rs2922446	8	134664999	C	A	−0.020	0.005	−3.961	7.57E-05
rs10007572	4	183691547	G	A	0.021	0.005	3.950	7.95E-05	TENM3	intron
rs1595373	11	16266740	G	A	−0.024	0.006	−3.946	8.07E-05	SOX6	intron
rs13241603	7	125901145	A	C	0.027	0.007	3.939	8.31E-05
rs10282703	7	125907965	A	G	0.027	0.007	3.939	8.31E-05
rs744270	6	89299046	A	G	0.041	0.010	3.916	9.14E-05
rs17046362	12	79483041	A	G	−0.098	0.025	−3.911	9.34E-05	SYT1	intron
rs17005224	12	79506862	A	G	−0.098	0.025	−3.911	9.34E-05	SYT1	intron
rs6881702	5	59277134	G	A	0.022	0.006	3.907	9.48E-05	PDE4D	intron
rs4542191	1	18813445	G	A	0.027	0.007	3.902	9.69E-05
rs10766314	11	16285515	G	A	−0.024	0.006	−3.902	9.69E-05	SOX6	intron
rs3985603	11	16283644	A	C	−0.024	0.006	−3.900	9.75E-05	SOX6	intron
rs486390	7	152783129	A	G	0.039	0.010	3.900	9.78E-05

Note. SNP = single nucleotide polymorphism; Chr = chromosome on which each SNP is located; Position = location in assembly GRCh37 (hg19). The two alleles at each locus are listed, with the minor allele listed first. Alleles are aligned to the forward strand of assembly GRCh37 (hg19). Beta = RFGLS regression coefficient; SE = standard error; df range = 4,449–4,452. Gene = nearest gene based on the NCBI database. If none is listed, then the SNP is located in an intergenic region. Class = SNP’s NCBI function class; intron = a noncoding variant.