DisGeNET - a database of gene-disease associations

List of shared variants

Parkinson Disease, C0030567

Disease: Schizophrenia

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
rs4919621	PITX3	0.851	0.080	10	102238914	intron variant	A/T	snv		0.66	4
rs1416580204	MOK	0.608	0.720	14	102250837	missense variant	C/T	snv	4.0E-06	7.0E-06	49
rs13107325	SLC39A8	0.776	0.520	4	102267552	missense variant	C/A;T	snv	4.0E-06; 4.5E-02		34
rs2494732	AKT1	0.763	0.240	14	104772855	intron variant	T/C	snv	0.50	0.47	11
rs1130214	AKT1	0.742	0.280	14	104793397	5 prime UTR variant	C/A	snv		0.31	12
rs671	ALDH2	0.529	0.840	12	111803962	missense variant	G/A	snv	1.9E-02	5.8E-03	116
rs16944	IL1B	0.531	0.920	2	112837290	upstream gene variant	A/G	snv		0.57	92
rs1143623	IL1B	0.677	0.440	2	112838252	upstream gene variant	C/G	snv		0.24	29
rs1800497	ANKK1	0.620	0.400	11	113400106	missense variant	G/A	snv	0.26	0.26	56
rs6277	DRD2	0.689	0.480	11	113412737	synonymous variant	G/A	snv	0.41	0.38	36
rs1076560	DRD2	0.776	0.120	11	113412966	intron variant	C/A	snv		0.16	11
rs2283265	DRD2	0.776	0.160	11	113414814	intron variant	C/A	snv		0.16	12
rs6280	DRD3	0.602	0.520	3	114171968	missense variant	C/T	snv	0.63	0.54	57
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs1801131	MTHFR	0.535	0.840	1	11794419	missense variant	T/G	snv	0.29	0.26	93
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs1801133	MTHFR	0.472	0.880	1	11796321	missense variant	G/A	snv	0.31	0.27	174
rs334558	LOC107986119 ; GSK3B	0.701	0.320	3	120094435	upstream gene variant	A/G	snv		0.51	20
rs1611115	DBH	0.732	0.280	9	133635393	upstream gene variant	T/C	snv		0.80	16
rs2007153	DBH	0.882	0.080	9	133638697	intron variant	T/C	snv		0.61	3
rs1108580	DBH	0.790	0.240	9	133639992	splice region variant	A/G	snv	0.45	0.54	9
rs2283123	DBH	0.882	0.080	9	133650175	intron variant	C/G;T	snv			3
rs1806201	GRIN2B	0.776	0.200	12	13564574	synonymous variant	G/A	snv	0.32	0.24	8
rs763059810	CXCR4	0.623	0.600	2	136115750	missense variant	T/C	snv	4.0E-06		41
rs4880213		0.827	0.160	9	137136549	upstream gene variant	C/G;T	snv			6