DisGeNET - a database of gene-disease associations

List of shared variants

Frontotemporal dementia, C0338451

Disease: Pick Disease of the Brain

Source: ALL

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
rs1012826460	MAPT	0.925	0.120	17	45971888	missense variant	G/A	snv	4.0E-06	1.4E-05	2
rs1295855402	MAPT	0.925	0.120	17	46024034	missense variant	C/T	snv		7.0E-06	2
rs1401496725	REG1A	0.925	0.120	2	79121657	missense variant	C/G;T	snv	8.0E-06; 8.0E-06		2
rs1417373701	SLCO6A1	0.925	0.120	5	102399606	missense variant	G/A	snv	4.0E-06		2
rs1804469	MSMB ; LOC105378287	0.925	0.120	10	46033495	missense variant	T/C	snv			2
rs63750711	MAPT	0.925	0.120	17	46018645	missense variant	A/T	snv			2
rs63751264	MAPT	0.925	0.120	17	46018726	missense variant	A/T	snv			2
rs751739883	MAPT	0.925	0.120	17	45983891	missense variant	C/T	snv	4.4E-06		2
rs767076633	TBK1	0.925	0.120	12	64484311	missense variant	T/C	snv	1.2E-05		2
rs773403329	SLCO6A1	0.925	0.120	5	102419925	missense variant	A/G	snv	4.1E-06	7.0E-06	2
rs774890160	MAPT	0.925	0.120	17	45974388	missense variant	T/C	snv	4.2E-06		2
rs964520949	PSPH	0.925	0.120	7	56019715	missense variant	C/T	snv	2.2E-04; 4.0E-06	1.9E-04	2
rs9897526	GRN	0.925	0.120	17	44349572	non coding transcript exon variant	G/A;C	snv	0.16		2
rs1182182524	MAPT	0.882	0.120	17	45983724	missense variant	T/G	snv		1.4E-05	3
rs139108915	PAX5	0.925	0.120	9	36840599	missense variant	G/A	snv	1.0E-05	9.8E-05	3
rs1595014		0.882	0.120	7	12148903	intergenic variant	T/A	snv		0.23	3
rs63750487	PSEN1	0.882	0.120	14	73192771	missense variant	C/T	snv			3
rs63750573	MAPT	0.882	0.120	17	46018627	missense variant	A/G	snv			3
rs63750905	MAPT	0.882	0.120	17	46018624	missense variant	G/T	snv			3
rs63751165	MAPT	0.925	0.120	17	46010401	missense variant	G/A;T	snv			3
rs760049824	MAPT	0.882	0.120	17	45983867	missense variant	T/A;C	snv	4.2E-06; 8.5E-06		3
rs767379602	VCP	0.882	0.120	9	35060823	missense variant	C/T	snv	1.2E-05	7.0E-06	3
rs1189501362	GSK3B	0.882	0.120	3	119863583	missense variant	G/A	snv		7.0E-06	4
rs1205185774	AHSA1	0.882	0.120	14	77469161	missense variant	C/T	snv			4
rs1235948930	MAPT	0.882	0.120	17	45983865	missense variant	C/T	snv		7.0E-06	4