DisGeNET - a database of gene-disease associations

List of shared variants

Tauopathies, C0949664

Disease: Presenile 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
rs34637584	LRRK2	0.583	0.480	12	40340400	missense variant	G/A	snv	5.3E-04	3.6E-04	78
rs63751273	MAPT	0.645	0.280	17	46010389	missense variant	C/T	snv			42
rs63750424	MAPT	0.677	0.240	17	46024061	missense variant	C/T	snv	1.6E-05		30
rs63750756	MAPT	0.716	0.200	17	46010324	missense variant	T/G	snv	2.6E-05		23
rs63751438	MAPT	0.776	0.120	17	46010388	missense variant	C/T	snv			16
rs242557	MAPT	0.752	0.200	17	45942346	intron variant	G/A	snv		0.36	12
rs63750376	MAPT	0.827	0.120	17	45996657	missense variant	G/T	snv			7
rs63750512	MAPT	0.827	0.160	17	46024010	missense variant	G/A;C	snv	1.2E-05		6
rs63750635	MAPT	0.851	0.120	17	46014286	missense variant	C/T	snv			5
rs763872192	CD36	0.882	0.080	7	80672000	missense variant	C/T	snv		2.8E-05	4