DisGeNET - a database of gene-disease associations

List of associated variants

Adenocarcinoma, Clear Cell, C0206681

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
rs231775	CTLA4	0.504	0.720	2	203867991	missense variant	A/G;T	snv	0.42; 4.0E-06		115
rs2476491	IL2RA	0.776	0.240	10	6053447	intron variant	A/T	snv		0.25	8
rs10795763	IL2RA	0.925	0.120	10	6054236	intron variant	G/T	snv		0.45	2
rs11256497	IL2RA	0.925	0.120	10	6045831	intron variant	G/A	snv		0.28	2
rs791587	IL2RA	0.925	0.120	10	6046736	intron variant	A/G	snv		0.51	2
rs141303532	FLCN	1.000	0.040	17	17221515	missense variant	G/A;T	snv	1.0E-04; 4.0E-06		1