rs3918188, NOS3

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.
Glaucoma, Primary Open Angle
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
222 0.776 0.280 7 151005693 intron variant C/A;T snv 0.020 2 2011 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.776 0.280 7 151005693 intron variant C/A;T snv 0.010 1.000 1 2016 2016
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.776 0.280 7 151005693 intron variant C/A;T snv 0.010 1.000 1 2016 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.776 0.280 7 151005693 intron variant C/A;T snv 0.010 1.000 1 2016 2016
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.776 0.280 7 151005693 intron variant C/A;T snv 0.010 1.000 1 2016 2016
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.776 0.280 7 151005693 intron variant C/A;T snv 0.010 1.000 1 2016 2016
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.776 0.280 7 151005693 intron variant C/A;T snv 0.010 1.000 1 2016 2016
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.776 0.280 7 151005693 intron variant C/A;T snv 0.010 1.000 1 2015 2015
Intraocular pressure disorder
CUI: C0595921
Disease: Intraocular pressure disorder
56 0.776 0.280 7 151005693 intron variant C/A;T snv 0.010 1.000 1 2011 2011
Pediatric Obesity
CUI: C2362324
Disease: Pediatric Obesity
67 0.776 0.280 7 151005693 intron variant C/A;T snv 0.010 1.000 1 2015 2015