DisGeNET - a database of gene-disease associations

List of shared variants

Amyotrophic Lateral Sclerosis, C0002736

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
rs1572931	RAB29 ; LOC105371702	0.925	0.080	1	205775090	splice region variant	C/A;T	snv		0.14	2
rs2275294	ZNF512B	0.925	0.080	20	63962894	intron variant	G/A	snv		0.25	3
rs267606929	OPTN	0.827	0.120	10	13132098	missense variant	A/G	snv			5
rs2736990	SNCA	0.882	0.080	4	89757390	intron variant	G/A;T	snv			4
rs34016896	LOC105374187	0.925	0.080	3	161275076	regulatory region variant	C/T	snv		0.28	3
rs356220	LOC105377329 ; SNCA	0.925	0.080	4	89720189	intron variant	T/A;C	snv			3
rs35801418	LRRK2	0.827	0.120	12	40321114	missense variant	A/G	snv			7
rs3794087	SLC1A2	0.851	0.120	11	35308068	intron variant	G/T	snv		0.20	6
rs3849942	C9orf72 ; LOC107987057	0.776	0.200	9	27543283	non coding transcript exon variant	T/A;C	snv			9
rs5848	FAM171A2 ; GRN	0.708	0.120	17	44352876	3 prime UTR variant	C/T	snv		0.41	17
rs591486	ERCC6L2	0.925	0.080	9	95887764	intron variant	A/G	snv		0.44	2
rs7224296	LRRC37A2 ; NSF	0.882	0.160	17	46722680	intron variant	G/A	snv		0.59	5