DisGeNET - a database of gene-disease associations

List of shared variants

Frontotemporal dementia, C0338451

Disease: Dementia

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
rs63750376	MAPT	0.827	0.120	17	45996657	missense variant	G/T	snv			7
rs201258663	LOC105375056 ; TREM2	0.807	0.320	6	41161457	missense variant	G/A	snv	5.6E-05	4.9E-05	6
rs63750512	MAPT	0.827	0.160	17	46024010	missense variant	G/A;C	snv	1.2E-05		6
rs63751068	PSEN1	0.827	0.120	14	73186920	missense variant	G/C;T	snv			6
rs80356715	TARDBP	0.807	0.120	1	11016874	missense variant	C/G;T	snv	8.0E-06; 2.2E-04		6
rs1057518919	PSEN1	0.851	0.120	14	73171023	missense variant	T/G	snv			5
rs63750635	MAPT	0.851	0.120	17	46014286	missense variant	C/T	snv			5
rs63750959	MAPT	0.827	0.200	17	45962351	missense variant	G/A;T	snv	6.0E-05		5
rs63751011	MAPT	0.925	0.120	17	46010418	intron variant	C/T	snv			4
rs63751399	PSEN1	0.882	0.120	14	73171047	missense variant	T/A;C	snv			3
rs901115236	CHCHD10 ; LOC107985577	0.882	0.120	22	23767531	missense variant	G/A;T	snv	1.5E-05; 1.5E-05		3