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.
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.080 0.875 8 2008 2018
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.070 0.714 7 2003 2016
Asthma
CUI: C0004096
Disease: Asthma
1536 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.060 0.667 6 2002 2012
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.060 1.000 6 2010 2018
Coronary Artery Vasospasm
CUI: C0010073
Disease: Coronary Artery Vasospasm
9 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.060 1.000 6 1998 2011
Eclampsia
CUI: C0013537
Disease: Eclampsia
38 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.060 0.833 6 2005 2019
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.060 1.000 6 2010 2018
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.060 0.833 6 2008 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.060 0.833 6 2004 2019
Obesity
CUI: C0028754
Disease: Obesity
1111 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.060 0.833 6 2004 2017
Polycystic Kidney, Autosomal Dominant
35 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.060 1.000 6 2002 2014
Pregnancy associated hypertension
CUI: C0852036
Disease: Pregnancy associated hypertension
43 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.060 1.000 6 2001 2016
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.050 0.800 5 2001 2007
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.050 0.800 5 2006 2012
High altitude pulmonary edema
CUI: C0340100
Disease: High altitude pulmonary edema
45 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.050 1.000 5 2002 2013
Intracranial Aneurysm
CUI: C0007766
Disease: Intracranial Aneurysm
150 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.050 0.600 5 2006 2015
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.050 0.800 5 2009 2016
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
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.050 0.800 5 2001 2015
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.040 1.000 4 2009 2015
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.040 1.000 4 2004 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.040 0.750 4 2014 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.040 0.750 4 2014 2019
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.030 1.000 3 2004 2012
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.030 0.667 3 2002 2015