DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Disease: Hypertensive disease ×

Variants associated to the Gene: RGS2 ×

Results per page

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
rs4606	RGS2	0.752	0.120	1	192812042	3 prime UTR variant	C/G;T	snv			16
rs2746071	RGS2	0.882	0.160	1	192808434	intron variant	A/G	snv		0.35	4
rs200339834	RGS2			1	192810186	missense variant	G/A	snv	1.2E-04	7.0E-05	1
rs34717272	RGS2			1	192810962	intron variant	TC/CT	mnv			1
rs74466425	RGS2			1	192809125	missense variant	G/C	snv	3.0E-04	2.0E-04	1
rs77790369	RGS2			1	192811493	missense variant	A/G	snv	1.6E-05		1