RGS2, regulator of G protein signaling 2, 5997

N. diseases: 109; N. variants: 8
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs74466425
rs74466425 		1 192809125 missense variant G/C snv 3.0E-04 2.0E-04
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs34717272
rs34717272 		1 192810962 intron variant TC/CT mnv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2008 2008