Correction: Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants

Table 3 Results of the rare variant analyses

Phenotype	ASD			Childhood autism			Asperger’s syndrome			ADHD			Schizophrenia
Gene	Number of variants	P-value	Rho	Number of variants	P-value	Rho	Number of variants	P-value	Rho	Number of variants	P-value	Rho	Number of variants	P-value	Rho
NOP9	63	0.067	0	47	0.165	0	50	0.103	0.5	57	0.233	0	47	0.115	0.3
KMT2D	465	0.250	0	355	0.670	0	368	0.545	1	437	0.737	1	337	0.136	1
RORB	14	0.243	1	11	0.033	1	12	0.894	1	14	0.300	1	11	0.396	1
ABCC13	1	0.138	NA	1	0.180	NA	1	0.584	NA	1	0.383	NA	1	0.079	NA
NDST4	46	0.009	0.4	43	0.189	1	44	0.124	0.4	49	0.238	1	45	0.148	1
FAT3	366	0.291	1	291	0.426	1	293	0.437	1	342	0.150	0.6	280	0.733	0
CMIP	22	0.402	1	18	1.000	1	18	0.637	0	23	1.000	0	17	0.715	0
PALB2	84	0.558	0	65	0.583	0	68	0.835	0	76	0.674	1	66	0.622	0
SCN9A	131	0.094	0	104	0.572	0	110	0.408	0	127	0.148	0	103	0.327	1
MUC6	32	0.911	1	28	0.810	0	29	1.000	1	33	0.843	1	29	0.864	1
NFXL1	26	0.519	1	13	0.695	0	15	0.235	1	17	0.849	1	13	0.559	0
OXR1	41	0.572	0.7	34	0.876	1	34	0.779	1	41	0.365	0	34	0.497	1
ATP2C2	167	0.880	1	120	0.448	0	132	0.288	1	161	0.226	1	116	0.821	1
SETBP1	109	0.850	1	90	0.884	1	92	0.593	1	109	1.000	1	86	0.380	1
CNTNAP2	122	0.527	0	96	0.280	0	104	0.763	1	120	0.235	0.9	93	0.840	0

The number of variants refers to the number of unique variants passing QC and count/frequency thresholds for each gene for each phenotype (this is not the variant count in individuals). Associations with summary statistics in italics were (only) nominally significant
ASD autism spectrum disorder, ADHD attention deficit/hyperactivity disorder, NA not applicable

ISSN: 1866-1955