NOS3, nitric oxide synthase 3, 4846

N. diseases: 706; N. variants: 39
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1799983
rs1799983 		0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.780 0.875 8 2007 2018
dbSNP: rs3918226
rs3918226 		0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 5 2017 2019
dbSNP: rs3918226
rs3918226 		0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 4 2015 2018
dbSNP: rs3918226
rs3918226 		0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 4 2017 2018
dbSNP: rs891511
rs891511 		7 151007755 intron variant G/A;C snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 2 2016 2019
dbSNP: rs3918198
rs3918198 		7 151009289 intron variant C/A snv 5.5E-03 2.0E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3918226
rs3918226 		0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
dbSNP: rs3918226
rs3918226 		0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs3918226
rs3918226 		0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs3918226
rs3918226 		0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs3918226
rs3918226 		0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs3918226
rs3918226 		0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs3918226
rs3918226 		0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs891511
rs891511 		7 151007755 intron variant G/A;C snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs891511
rs891511 		7 151007755 intron variant G/A;C snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs891511
rs891511 		7 151007755 intron variant G/A;C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2070744
rs2070744 		0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C3149657
Disease: CORONARY ARTERY SPASM 1, SUSCEPTIBILITY TO
CORONARY ARTERY SPASM 1, SUSCEPTIBILITY TO 		0.700 0
dbSNP: rs1799983
rs1799983 		0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.100 0.849 53 1998 2019
dbSNP: rs1799983
rs1799983 		0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.100 0.927 41 1999 2017
dbSNP: rs1799983
rs1799983 		0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.100 0.974 39 1998 2020
dbSNP: rs1799983
rs1799983 		0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.100 0.917 36 1998 2019
dbSNP: rs1799983
rs1799983 		0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.100 0.917 24 1998 2019
dbSNP: rs1799983
rs1799983 		0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.100 1.000 20 2005 2019
dbSNP: rs1799983
rs1799983 		0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.100 0.895 19 1998 2017
dbSNP: rs1799983
rs1799983 		0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.100 0.895 19 2002 2020