rs1799983, NOS3

N. diseases: 246
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.
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2008 2008
Renal Artery Stenosis
CUI: C0035067
Disease: Renal Artery Stenosis
8 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2008 2008
Rhinitis
CUI: C0035455
Disease: Rhinitis
20 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2008 2008
Skin lesion
CUI: C0037284
Disease: Skin lesion
52 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2008 2008
Subarachnoid Hemorrhage
CUI: C0038525
Disease: Subarachnoid Hemorrhage
26 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2008 2008
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2008 2009
Infarction, Lacunar
CUI: C0333559
Disease: Infarction, Lacunar
18 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2004 2009
ABLEPHARON-MACROSTOMIA SYNDROME
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
14 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009
Acute mountain sickness
CUI: C0238284
Disease: Acute mountain sickness
3 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009
Bacteremia
CUI: C0004610
Disease: Bacteremia
7 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009
Chronic Kidney Insufficiency
CUI: C0403447
Disease: Chronic Kidney Insufficiency
12 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009
Cone-Rod Dystrophy 2
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
51 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009
Encephalitis, St. Louis
CUI: C0014060
Disease: Encephalitis, St. Louis
34 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1 2009 2009
First myocardial infarction
CUI: C1273976
Disease: First myocardial infarction
7 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1 2009 2009
Frontotemporal Lobar Degeneration
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
54 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009
GRN-related frontotemporal dementia
CUI: C3811918
Disease: GRN-related frontotemporal dementia
20 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009
Malaria
CUI: C0024530
Disease: Malaria
148 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009
Malaria, Cerebral
CUI: C0024534
Disease: Malaria, Cerebral
34 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009
Resistant hypertensive disorder
CUI: C0745130
Disease: Resistant hypertensive disorder
14 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.050 1.000 5 2002 2010
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.030 1.000 3 2000 2010
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2005 2010
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2009 2010
Thromboangiitis Obliterans
CUI: C0040021
Disease: Thromboangiitis Obliterans
16 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 0.500 2 2002 2010
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2010 2010