rs633185, ARHGAP42

N. diseases: 10
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.925 0.080 11 100722807 intron variant G/A;C snv 0.700 1.000 8 2011 2018
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.925 0.080 11 100722807 intron variant G/A;C snv 0.700 1.000 6 2011 2018
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
344 0.925 0.080 11 100722807 intron variant G/A;C snv 0.700 1.000 3 2011 2018
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 0.925 0.080 11 100722807 intron variant G/A;C snv 0.800 1.000 2 2011 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.925 0.080 11 100722807 intron variant G/A;C snv 0.800 1.000 2 2011 2018
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
535 0.925 0.080 11 100722807 intron variant G/A;C snv 0.700 1.000 1 2018 2018
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.925 0.080 11 100722807 intron variant G/A;C snv 0.700 1.000 1 2019 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.925 0.080 11 100722807 intron variant G/A;C snv 0.700 1.000 1 2018 2018
Diastolic blood pressure measurement
81 0.925 0.080 11 100722807 intron variant G/A;C snv 0.700 1.000 1 2011 2011
Systolic blood pressure measurement
CUI: C1306620
Disease: Systolic blood pressure measurement
95 0.925 0.080 11 100722807 intron variant G/A;C snv 0.700 1.000 1 2011 2011