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.
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 hepatitis
CUI: C0267797
Disease: Acute hepatitis
2 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2014 2014
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
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2013 2013
Aggressive periodontitis, generalized
CUI: C1719495
Disease: Aggressive periodontitis, generalized
16 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2006 2006
Alcohol abuse
CUI: C0085762
Disease: Alcohol abuse
24 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2006 2006
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
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
Aneurysm, Ruptured
CUI: C0162869
Disease: Aneurysm, Ruptured
1 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2011 2011
Asthenozoospermia
CUI: C0403823
Disease: Asthenozoospermia
17 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1 2015 2015
Ataxia with vitamin E deficiency
CUI: C1848533
Disease: Ataxia with vitamin E deficiency
32 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
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
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2015 2015
Avascular Necrosis of Femur Head
CUI: C0410480
Disease: Avascular Necrosis of Femur Head
20 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2014 2014
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
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1 2015 2015
Blind Loop Syndrome
CUI: C0005750
Disease: Blind Loop Syndrome
3 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2012 2012
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
Bronchopulmonary Dysplasia
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
112 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2015 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1 2019 2019
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2016 2016
Carcinoma of urinary bladder, invasive
CUI: C1827293
Disease: Carcinoma of urinary bladder, invasive
14 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
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
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