DisGeNET - a database of gene-disease associations

List of shared variants

Neurodegenerative Disorders, C0524851

Disease: Parkinson Disease

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
rs156697	GSTO2	0.672	0.560	10	104279427	missense variant	A/G;T	snv	0.35		25
rs3173615	TMEM106B	0.807	0.200	7	12229791	missense variant	C/A;G	snv	0.49		12
rs35801418	LRRK2	0.827	0.120	12	40321114	missense variant	A/G	snv			7
rs3857059	SNCA	1.000	0.040	4	89754087	intron variant	A/G;T	snv			2
rs397515634	UCHL1-AS1 ; UCHL1	0.925	0.040	4	41256996	missense variant	A/C	snv	4.0E-06		3
rs431905511	SNCA	0.827	0.080	4	89828154	missense variant	C/T	snv			9
rs75932628	LOC105375056 ; TREM2	0.662	0.480	6	41161514	missense variant	C/A;T	snv	6.8E-05; 2.6E-03		28
rs759834365	BDNF-AS ; BDNF	0.448	0.760	11	27658456	missense variant	C/T	snv	1.2E-05		237