DisGeNET - a database of gene-disease associations

List of associated variants

Psychotic Disorders, C0033975

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
rs3800373	LOC101929309 ; FKBP5	0.752	0.200	6	35574699	3 prime UTR variant	C/A	snv		0.68	22
rs1555939456	RPS6KA3	0.851	0.200	X	20187956	missense variant	T/C	snv			21
rs1344706	ZNF804A	0.701	0.160	2	184913701	intron variant	A/C;T	snv			21
rs2023239	CNR1	0.724	0.160	6	88150763	intron variant	T/C	snv		0.21	20
rs2424913	DNMT3B	0.708	0.440	20	32786453	intron variant	C/T	snv	0.56	0.53	18
rs16147	LOC107986777 ; NPY	0.695	0.400	7	24283791	upstream gene variant	T/C	snv		0.48	18
rs3730358	AKT1	0.724	0.360	14	104780070	intron variant	G/A;C	snv	0.16; 4.0E-03		14
rs1625579	MIR137HG	0.763	0.160	1	98037378	intron variant	G/T	snv		0.78	14
rs2251219	SMIM4 ; PBRM1	0.732	0.120	3	52550771	synonymous variant	T/C;G	snv	0.39; 4.0E-06	0.34	14
rs135745		0.763	0.200	22	38287631	downstream gene variant	G/C	snv		0.48	13
rs6994992	NRG1	0.790	0.120	8	31638065	upstream gene variant	C/A;T	snv			13
rs1130214	AKT1	0.742	0.280	14	104793397	5 prime UTR variant	C/A	snv		0.31	12
rs2494732	AKT1	0.763	0.240	14	104772855	intron variant	T/C	snv	0.50	0.47	11
rs1076560	DRD2	0.776	0.120	11	113412966	intron variant	C/A	snv		0.16	11
rs3213207	DTNBP1	0.776	0.120	6	15627871	intron variant	T/C	snv		8.7E-02	11
rs1200746244	MTHFR	0.807	0.080	1	11801287	missense variant	C/T	snv	4.0E-06	7.0E-06	11
rs737865	TXNRD2 ; COMT	0.763	0.240	22	19942598	intron variant	A/G	snv		0.23	11
rs886424	LINC00243	0.776	0.320	6	30814225	non coding transcript exon variant	C/T	snv	7.1E-02	8.7E-02	10
rs5174	LRP8	0.776	0.240	1	53247055	missense variant	C/T	snv	0.29	0.28	10
rs934945	PER2	0.827	0.200	2	238246412	missense variant	C/T	snv	0.21	0.15	10
rs9834970		0.790	0.080	3	36814539	downstream gene variant	T/C	snv		0.45	9
rs1535255	CNR1	0.807	0.120	6	88151489	intron variant	T/G	snv		0.21	8
rs1800955	DRD4	0.827	0.160	11	636784	upstream gene variant	T/C;G	snv			8
rs2498804	LOC102723342 ; SIVA1 ; LOC107987209	0.827	0.160	14	104766758	intron variant	C/A;T	snv	0.40	0.33	8
rs4650608		0.851	0.040	1	78772330	intergenic variant	T/C	snv		0.29	7