DisGeNET - a database of gene-disease associations

List of shared variants

Parkinson Disease, C0030567

Disease: Corpuscular Hemoglobin Concentration Mean

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
rs1864325	MAPT	0.882	0.160	17	45900461	intron variant	C/T	snv		0.14	5
rs393152	LINC02210 ; LINC02210-CRHR1	0.851	0.160	17	45641777	non coding transcript exon variant	A/G	snv	0.18	0.29	5
rs8070723	MAPT	0.851	0.240	17	46003698	intron variant	A/G	snv		0.18	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
rs12373139	MAPT-AS1 ; SPPL2C	0.925	0.120	17	45846764	missense variant	G/A	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
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
rs199533	NSF ; LRRC37A2	0.925	0.120	17	46751565	synonymous variant	G/A	snv	0.13	0.13	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
rs10445337	MAPT	0.925	0.120	17	45990034	missense variant	T/C	snv	0.15	0.15	3
rs1052587	MAPT	0.925	0.120	17	46025238	3 prime UTR variant	T/C	snv		0.14	3
rs1078268	STH ; MAPT	0.925	0.120	17	45998535	intron variant	A/G	snv		0.15	3
rs12185235	MAPT-AS1 ; SPPL2C	0.925	0.120	17	45846337	synonymous variant	C/T	snv	0.14	0.14	3
rs12185268	MAPT-AS1 ; SPPL2C	0.851	0.160	17	45846317	missense variant	A/G	snv	0.15	0.14	3
rs17563986	MAPT	1.000	0.040	17	45913906	intron variant	A/G	snv		0.14	3
rs17574228	KANSL1 ; MAPT	0.925	0.120	17	46027143	3 prime UTR variant	T/C	snv		0.14	3
rs17574604	KANSL1	0.925	0.120	17	46034247	synonymous variant	A/G	snv	0.15	0.14	3
rs17577094	KANSL1	0.925	0.120	17	46110126	intron variant	A/G	snv		0.14	3
rs17650901	MAPT	0.925	0.120	17	45962325	5 prime UTR variant	A/G	snv	0.14	0.14	3
rs17652121	MAPT	0.925	0.120	17	45996607	synonymous variant	T/C	snv	0.14	0.15	3
rs17763596	SPPL2C ; MAPT-AS1	0.925	0.120	17	45843844	non coding transcript exon variant	G/T	snv		0.14	3
rs1800547	MAPT	0.925	0.120	17	45974480	non coding transcript exon variant	A/G	snv	0.15	0.14	3