Table 2.

Association analysis of rare missense variant

variant	Genome data			Case (SCZ+ASD)					Control
p.A33T	positiona	Transcript variant		Genotype countb	MAF	P-valuec	Odds radio		Genotype count	MAF
	21:34399267	c.97G>A		0/0/1827	0	N/A	N/A		0/1/1472	0.0003

SCZ: schizophrenia

ASD: autism spectrum disorders

MAF: minor allele frequency

^a Genomic position based on NCBI build GRCh 37.p13 (Transcript ID ENST00000371236.2).

^b Genotype count; homozygote of minor allele/heterozygote/homozygote of major allele.

^c P-values were calculated with Fisher’s exact test (2 × 2 contingency table, one-tail).