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.
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
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
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
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
Spina Bifida
CUI: C0080178
Disease: Spina Bifida
61 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2004 2007
Atherosclerotic renal artery stenosis
CUI: C0340557
Disease: Atherosclerotic renal artery stenosis
4 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2004 2004
CARCINOMA OF VULVA
CUI: C0677055
Disease: CARCINOMA OF VULVA
2 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1 2004 2004
Hypertension, Renovascular
CUI: C0020545
Disease: Hypertension, Renovascular
8 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2004 2004
Malignant neoplasm of vulva
CUI: C0375071
Disease: Malignant neoplasm of vulva
2 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1 2004 2004
Miscarriage
CUI: C4552766
Disease: Miscarriage
56 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1 2004 2004
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2004 2004
Renal vascular disorder
CUI: C0268790
Disease: Renal vascular disorder
6 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2004 2004
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.100 1.000 20 2005 2019
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
Premature coronary artery atherosclerosis
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
43 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.030 1.000 3 2005 2017
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
Conotruncal defect
CUI: C1853238
Disease: Conotruncal defect
45 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2005 2011
Alzheimer disease, familial, type 3
CUI: C1843013
Disease: Alzheimer disease, familial, type 3
124 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2005 2005
Cleft Lip with or without Cleft Palate
CUI: C0810364
Disease: Cleft Lip with or without Cleft Palate
50 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2005 2005
Cleft lip, isolated
CUI: C1837217
Disease: Cleft lip, isolated
2 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2005 2005
Cockayne Syndrome, Type I
CUI: C0751039
Disease: Cockayne Syndrome, Type I
42 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2005 2005
Coronary Occlusion
CUI: C0151814
Disease: Coronary Occlusion
1 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2005 2005
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2005 2005
Hypertrophic obstructive cardiomyopathy
CUI: C4551472
Disease: Hypertrophic obstructive cardiomyopathy
90 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2005 2005