. Author manuscript; available in PMC: 2021 Jun 1.

Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2020 Apr 8;183(4):227–233. doi: 10.1002/ajmg.b.32781

TABLE 1.

Contingency tables and Fischer's exact test statistic values for neuropsychiatric phenotypes versus MYT1L variants

		Neuropsychiatric phenotype
		ASD^a		SCHZ^b		ID^c
		+	−	+	−	+	−
MYT1L variants	Duplication	6	21	10	17	6	21
	Loss of function	22	29	0	51	46	5

Abbreviations: ASD, autism spectrum disorder; dup, duplication; ID, intellectual disability; lof, loss of function; SCHZ, schizophrenia.

ASD+/ASD-Fischer's exact test statistic value, versus dup/lof = .0849, NOT significant. (This pertains to all reported variants and should not infer that specific sequence variants would not reach the statistical threshold individually for an effect on these phenotypes.)

SCHZ+/SCHZ-Fischer's exact test statistic value, versus dup/lof < .0001, Significant.

ID+/ID-Fischer's exact test statistic value, versus dup/lof < .0001, Significant.