DisGeNET - a database of gene-disease associations

List of shared variants

Parkinson Disease, C0030567

Disease: Lung Diseases, Interstitial

Source: INFERRED ×

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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
rs393152	LINC02210 ; LINC02210-CRHR1	0.851	0.160	17	45641777	non coding transcript exon variant	A/G	snv	0.18	0.29	6
rs8070723	MAPT	0.851	0.240	17	46003698	intron variant	A/G	snv		0.18	6
rs12373139	MAPT-AS1 ; SPPL2C	0.925	0.120	17	45846764	missense variant	G/A	snv	0.15	0.14	4
rs17563986	MAPT	1.000	0.040	17	45913906	intron variant	A/G	snv		0.14	4
rs199533	NSF ; LRRC37A2	0.925	0.120	17	46751565	synonymous variant	G/A	snv	0.13	0.13	4
rs546433642	KANSL1	0.925	0.120	17	46172742	intron variant	T/C;G	snv			4
rs549599956	KANSL1	0.925	0.120	17	46169798	intron variant	A/G	snv			4
rs169201	NSF ; LRRC37A2	0.925	0.160	17	46712837	intron variant	A/G	snv		0.13	3
rs1981997	MAPT	1.000	0.040	17	45979401	non coding transcript exon variant	G/A	snv		0.14	3
rs2668692	KANSL1	1.000	0.040	17	46215654	intron variant	G/A;T	snv			3
rs415430	WNT3 ; LRRC37A2	1.000	0.040	17	46781778	intron variant	C/T	snv		0.84	3
rs7215239	LINC02210-CRHR1	1.000	0.040	17	45690407	intron variant	T/C	snv		0.30	3