DisGeNET - a database of gene-disease associations

List of shared variants

Child Development Disorders, Pervasive, C0008074

Disease: Psychotic Disorders

Source: ALL

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Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	DSI _v	DPI _v	Chr	Position	Consequence	Alleles	Class	AF EXOME	AF GENOME	Num. diseases
rs1006737	CACNA1C	0.695	0.120	12	2236129	intron variant	G/A	snv		0.36	27
rs1625579	MIR137HG	0.763	0.160	1	98037378	intron variant	G/T	snv		0.78	14
rs10994359	ANK3	0.827	0.040	10	60462349	intron variant	T/C	snv		8.0E-02	7
rs12966547	LOC105372125	0.827	0.040	18	55084786	intergenic variant	G/A	snv		0.39	7
rs4650608		0.851	0.040	1	78772330	intergenic variant	T/C	snv		0.29	7
rs2007044	CACNA1C	0.882	0.040	12	2235794	intron variant	A/G	snv		0.50	6