Table 2.

All Significant and Suggestive Genes From the Gene-based Linkage Analysis

CHR	POS	GENE	CUMUL LOD	HLOD	VARIANTS
7	48.34	CRHR2	3.98	4.06	All
7	50.78	AVL9	3.99	3.99	All
9	59.79	DNAI1	2.81	2.81	All
7	52.59	NPSR1-AS1	2.74	2.74	All
7	52.05	BMPER	1.86	2.73	All
20	54.18	BPIFA2	2.64	2.65	All
7	54.00	SEPT7	2.34	2.61	All
20	28.26	PAK7	1.75	2.47	All
1	49.16	EPHB2	2.44	2.44	All
9	43.87	FOCAD	2.14	2.37	All
18	8.08	SMCHD1	2.37	2.37	All
3	39.61	EFHB	1.77	2.36	All
7	48.59	INMT-FAM188B	2.35	2.35	Rare
13	36.59	CSNK1A1L	2.15	2.35	All
6	92.24	COL12A1	2.34	2.34	All
13	52.86	SETDB2	1.94	2.30	All
7	50.30	PDE1C	2.21	2.21	All
20	55.10	CEP250	1.93	2.10	All
14	97.59	SERPINA9	1.35	2.09	All
4	9.39	EVC	0.92	2.08	All
7	54.69	KIAA0895	1.34	2.04	All
7	46.21	LOC646762	1.49	1.99	All
7	48.61	FAM188B	1.99	1.99	Rare
9	111.62	ZNF462	1.95	1.95	All
4	9.39	EVC	1.93	1.93	Rare
6	178.62	PACRG	0.72	1.92	All
1	49.16	EPHB2	1.92	1.92	All
7	50.30	PDE1C	0.31	1.91	All
9	123.13	AKNA	1.90	1.90	Rare

The list of all significant and suggestive genes from the gene-based linkage analyses, as sorted by HLOD. Here the headers represent: CHR = chromosome, POS = genetic position in cM of the gene, GENE = gene, CUMUL LOD = cumulative LOD score for the gene across all 106 families, HLOD = heterogeneity LOD score for the gene across all 106 families, VARIANTS = type of variants used in this test (All = all variants were used, Rare = only rare variants (MAF ≤ 0.05) were used).