ARHGAP42, Rho GTPase activating protein 42, 143872

N. diseases: 25; N. variants: 14
Disease: Coronary Artery Disease ×
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: rs4754698
rs4754698 		1.000 0.040 11 100761177 intron variant C/A;G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs604723
rs604723 		1.000 0.040 11 100739815 intron variant T/C snv 0.78
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs633185
rs633185 		0.925 0.080 11 100722807 intron variant G/A;C snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7947761
rs7947761 		1.000 0.040 11 100753868 intron variant A/G snv 0.26
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018