DisGeNET - a database of gene-disease associations

List of shared variants

Essential Tremor, C0270736

Disease: Parkinson Disease, Familial, Type 1

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
rs34778348	LRRK2 ; LOC105369736	0.742	0.120	12	40363526	missense variant	G/A	snv	1.7E-03	5.8E-04	15
rs33949390	LRRK2	0.776	0.160	12	40320043	missense variant	G/A;C;T	snv	1.6E-04; 1.9E-03; 8.0E-06		9
rs35870237	LRRK2	0.763	0.120	12	40340404	missense variant	T/C	snv			9
rs387907571	DNAJC13	0.827	0.080	3	132477995	missense variant	A/G	snv	4.2E-06	3.5E-05	6
rs864309650	CHCHD2	0.851	0.040	7	56104344	missense variant	G/A	snv			4