rs11771443, NOS3

N. diseases: 8
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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
Glaucoma, Primary Open Angle
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
222 0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 0.010 1.000 1 2011 2011
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
59 0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 0.010 1.000 1 2017 2017
Intraocular pressure disorder
CUI: C0595921
Disease: Intraocular pressure disorder
56 0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 0.010 1.000 1 2011 2011