DisGeNET - a database of gene-disease associations

List of associated variants

Parkinson Disease, C0030567

Source: GWASDB ×

Results per page

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
rs1800562	LOC108783645 ; HFE	0.435	0.880	6	26092913	missense variant	G/A	snv	3.3E-02	3.8E-02	14
rs671	ALDH2	0.529	0.840	12	111803962	missense variant	G/A	snv	1.9E-02	5.8E-03	10
rs646776	CELSR2	0.752	0.240	1	109275908	downstream gene variant	C/T	snv		0.74	10
rs1799945	LOC108783645 ; HFE	0.452	0.760	6	26090951	missense variant	C/G;T	snv	0.11	0.10	10
rs13107325	SLC39A8	0.776	0.520	4	102267552	missense variant	C/A;T	snv	4.0E-06; 4.5E-02		8
rs1229984	ADH1B	0.570	0.560	4	99318162	missense variant	T/C;G	snv	0.90		6
rs12413409	CNNM2	0.790	0.200	10	102959339	intron variant	G/A	snv		9.0E-02	6
rs660895	HLA-DRB1	0.752	0.360	6	32609603	intergenic variant	A/G	snv		0.19	6
rs3129882	HLA-DRA	0.807	0.240	6	32441753	intron variant	G/A	snv		0.56	5
rs393152	LINC02210 ; LINC02210-CRHR1	0.851	0.160	17	45641777	non coding transcript exon variant	A/G	snv	0.18	0.29	5
rs1864325	MAPT	0.882	0.160	17	45900461	intron variant	C/T	snv		0.14	5
rs8070723	MAPT	0.851	0.240	17	46003698	intron variant	A/G	snv		0.18	5
rs2070600	AGER	0.561	0.760	6	32183666	missense variant	C/T	snv	5.3E-02	3.6E-02	4
rs6265	BDNF ; BDNF-AS	0.436	0.760	11	27658369	missense variant	C/T	snv	0.19	0.15	4
rs546433642	KANSL1	0.925	0.120	17	46172742	intron variant	T/C;G	snv			4
rs549599956	KANSL1	0.925	0.120	17	46169798	intron variant	A/G	snv			4
rs17651549	MAPT	0.882	0.160	17	45983912	missense variant	C/T	snv	0.15	0.14	4
rs17690703	MAPT-AS1	0.882	0.160	17	45847931	intron variant	C/T	snv		0.18	4
rs12373139	MAPT-AS1 ; SPPL2C	0.925	0.120	17	45846764	missense variant	G/A	snv	0.15	0.14	4
rs1805007	MC1R	0.695	0.280	16	89919709	missense variant	C/A;G;T	snv	4.4E-02		4
rs199533	NSF ; LRRC37A2	0.925	0.120	17	46751565	synonymous variant	G/A	snv	0.13	0.13	4
rs12185233	SPPL2C ; MAPT-AS1	0.882	0.160	17	45846288	missense variant	G/A;C	snv	9.5E-05; 0.15		4
rs12373123	SPPL2C ; MAPT-AS1	0.882	0.160	17	45846707	missense variant	T/C	snv	0.15	0.14	4
rs12373142	SPPL2C ; MAPT-AS1	0.851	0.200	17	45846834	missense variant	C/G;T	snv	0.15		4
rs2395163		0.882	0.160	6	32420032	intergenic variant	T/C	snv		0.17	3