DisGeNET - a database of gene-disease associations

List of associated variants

Autosomal dominant late onset Parkinson disease, C4274355

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
rs35870237	LRRK2	0.763	0.120	12	40340404	missense variant	T/C	snv			9
rs188286943	VPS35	0.776	0.160	16	46662452	missense variant	C/T	snv			9
rs35801418	LRRK2	0.827	0.120	12	40321114	missense variant	A/G	snv			7
rs3743928	ORC6 ; VPS35	1.000	0.040	16	46689167	5 prime UTR variant	C/A;G;T	snv	8.1E-05; 4.5E-06; 3.2E-05; 3.3E-03		1