DisGeNET - a database of gene-disease associations

List of shared variants

Parkinson Disease, C0030567

Disease: Alopecia, Male Pattern

Source: INFERRED ×

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
rs1864325	MAPT	0.882	0.160	17	45900461	intron variant	C/T	snv		0.14	6
rs12373142	SPPL2C ; MAPT-AS1	0.851	0.200	17	45846834	missense variant	C/G;T	snv	0.15		5
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
rs17651549	MAPT	0.882	0.160	17	45983912	missense variant	C/T	snv	0.15	0.14	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
rs12185235	MAPT-AS1 ; SPPL2C	0.925	0.120	17	45846337	synonymous variant	C/T	snv	0.14	0.14	3
rs17650901	MAPT	0.925	0.120	17	45962325	5 prime UTR variant	A/G	snv	0.14	0.14	3
rs1800547	MAPT	0.925	0.120	17	45974480	non coding transcript exon variant	A/G	snv	0.15	0.14	3