DisGeNET - a database of gene-disease associations

List of shared variants

Frontotemporal dementia, C0338451

Disease: Parkinsonian Disorders

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
rs104893877	SNCA	0.614	0.360	4	89828149	missense variant	C/T	snv			59
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
rs143624519	MAPT	0.724	0.240	17	45991484	missense variant	G/A;T	snv	1.5E-03; 1.2E-05		17
rs63751438	MAPT	0.776	0.120	17	46010388	missense variant	C/T	snv			16
rs367543041	TARDBP	0.742	0.200	1	11022553	missense variant	G/A;C	snv	3.0E-05		15
rs63750590	PSEN1	0.790	0.120	14	73186860	missense variant	A/G	snv			10
rs767543900	MAPT	0.790	0.120	17	45971879	missense variant	A/C;G	snv	4.0E-06		10
rs34015634	LRRK2	0.851	0.120	12	40340380	missense variant	T/C	snv	3.2E-05	1.4E-05	8
rs63750416	MAPT	0.851	0.120	17	46010373	missense variant	A/C	snv			7
rs267604921	MAPT	0.925	0.160	17	45993953	missense variant	C/A;G;T	snv	6.3E-05; 2.5E-04; 5.3E-06		3
rs63751165	MAPT	0.925	0.120	17	46010401	missense variant	G/A;T	snv			3