RGS3, regulator of G protein signaling 3, 5998

N. diseases: 21; N. variants: 4
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: rs10981835
rs10981835 		9 113587018 intron variant G/A snv 0.12
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs111296842
rs111296842 		9 113448483 intron variant C/G snv 3.7E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs113800797
rs113800797 		9 113596258 intron variant C/T snv 6.1E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs12341266
rs12341266 		1.000 0.040 9 113594236 missense variant A/C;G snv 0.93
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		Cardiovascular Diseases 0.700 1.000 1 2013 2013