Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.050 1.000 5 2013 2019
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.040 0.750 4 2013 2017
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.040 1.000 4 2011 2012
dbSNP: rs3918226
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.040 1.000 4 2012 2015
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.030 1.000 3 2016 2019
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.030 1.000 3 2014 2019
dbSNP: rs1800779
rs1800779
NOS3
0.763 0.320 7 150992855 intron variant G/A;C snv
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
Hypoxic-Ischemic Encephalopathy 		0.020 1.000 2 2011 2014
dbSNP: rs1800780
rs1800780
NOS3
0.925 0.120 7 151001791 intron variant A/G snv 0.58 0.56
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.020 1.000 2 2013 2014
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia 		0.020 1.000 2 2015 2015
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		0.020 1.000 2 2008 2017
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.020 1.000 2 2018 2019
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
Hypoxic-Ischemic Encephalopathy 		0.020 1.000 2 2014 2016
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0152136
Disease: Low Tension Glaucoma
Low Tension Glaucoma 		0.020 1.000 2 2012 2017
dbSNP: rs3918181
rs3918181
NOS3
0.925 0.120 7 151004695 intron variant G/A snv 0.35
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.020 0.500 2 2013 2014
dbSNP: rs3918188
rs3918188
NOS3
0.776 0.280 7 151005693 intron variant C/A;T snv
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle 		0.020 < 0.001 2 2011 2011
dbSNP: rs743506
rs743506
NOS3
0.925 0.120 7 151009827 intron variant G/A;C snv
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.020 1.000 2 2011 2012
dbSNP: rs869109213
rs869109213
NOS3
0.790 0.200 7 150997269 intron variant GGGGGTGAGGAAGTCTAGACCTGCTGCG/A delins
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.020 1.000 2 2018 2019
dbSNP: rs1541861
rs1541861
NOS3
0.925 0.040 7 151000245 intron variant C/A snv 0.70
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2006 2006
dbSNP: rs1541861
rs1541861
NOS3
0.925 0.040 7 151000245 intron variant C/A snv 0.70
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2016 2016
dbSNP: rs1800779
rs1800779
NOS3
0.763 0.320 7 150992855 intron variant G/A;C snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 < 0.001 1 2016 2016
dbSNP: rs1800779
rs1800779
NOS3
0.763 0.320 7 150992855 intron variant G/A;C snv
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
Uveomeningoencephalitic Syndrome 		0.010 < 0.001 1 2016 2016
dbSNP: rs1800779
rs1800779
NOS3
0.763 0.320 7 150992855 intron variant G/A;C snv
CUI: C0018801
Disease: Heart failure
Heart failure 		0.010 1.000 1 2012 2012
dbSNP: rs1800779
rs1800779
NOS3
0.763 0.320 7 150992855 intron variant G/A;C snv
CUI: C1531624
Disease: Cardioembolic stroke
Cardioembolic stroke 		0.010 1.000 1 2015 2015
dbSNP: rs1800779
rs1800779
NOS3
0.763 0.320 7 150992855 intron variant G/A;C snv
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.010 1.000 1 2012 2012
dbSNP: rs1800779
rs1800779
NOS3
0.763 0.320 7 150992855 intron variant G/A;C snv
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.010 1.000 1 2013 2013