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 Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2009 2012
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 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
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
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
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
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
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.080 0.875 8 2000 2015
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2013 2017
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
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
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.100 0.818 11 1999 2018
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
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
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
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.100 0.818 11 1999 2018
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