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.
Brain Infarction
CUI: C0751955
Disease: Brain Infarction
11 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2000 2000
Cor pulmonale
CUI: C0034072
Disease: Cor pulmonale
2 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2000 2000
Stroke, Lacunar
CUI: C3178801
Disease: Stroke, Lacunar
11 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2000 2000
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2001 2001
HYPERTENSION, RESISTANT TO CONVENTIONAL THERAPY
CUI: C1834155
Disease: HYPERTENSION, RESISTANT TO CONVENTIONAL THERAPY
1 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2001 2001
Macroangiopathy
CUI: C1096293
Disease: Macroangiopathy
6 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2001 2001
Maternal hypertension
CUI: C0565599
Disease: Maternal hypertension
22 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2001 2001
Allergic asthma
CUI: C0155877
Disease: Allergic asthma
55 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2002 2002
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2002 2002
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2002 2002
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2002 2002
IgE-mediated allergic asthma
CUI: C1827849
Disease: IgE-mediated allergic asthma
46 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2002 2002
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2002 2002
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2002 2002
POLYCYSTIC KIDNEY DISEASE 1
CUI: C3149841
Disease: POLYCYSTIC KIDNEY DISEASE 1
134 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2003 2003
Rheumatism
CUI: C0035435
Disease: Rheumatism
19 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2003 2003
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
Coronary spastic angina
CUI: C0948698
Disease: Coronary spastic angina
1 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 1998 2005
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