rs1800779, NOS3

N. diseases: 9
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.
Hypoxic-Ischemic Encephalopathy
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
12 0.763 0.320 7 150992855 intron variant G/A;C snv 0.020 1.000 2 2011 2014
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.763 0.320 7 150992855 intron variant G/A;C snv 0.010 1 2016 2016
Cardioembolic stroke
CUI: C1531624
Disease: Cardioembolic stroke
28 0.763 0.320 7 150992855 intron variant G/A;C snv 0.010 1.000 1 2015 2015
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.763 0.320 7 150992855 intron variant G/A;C snv 0.010 1.000 1 2013 2013
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.763 0.320 7 150992855 intron variant G/A;C snv 0.010 1.000 1 2012 2012
Glaucoma, Primary Open Angle
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
222 0.763 0.320 7 150992855 intron variant G/A;C snv 0.010 1.000 1 2010 2010
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.763 0.320 7 150992855 intron variant G/A;C snv 0.010 1.000 1 2012 2012
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.763 0.320 7 150992855 intron variant G/A;C snv 0.010 1.000 1 2013 2013
Uveomeningoencephalitic Syndrome
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
27 0.763 0.320 7 150992855 intron variant G/A;C snv 0.010 1 2016 2016