rs2070744, NOS3

N. diseases: 54
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.
CORONARY ARTERY SPASM 1, SUSCEPTIBILITY TO
1 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.700 0
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.050 1.000 5 2013 2019
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.040 0.750 4 2013 2017
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.040 1.000 4 2011 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.030 1.000 3 2016 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.030 1.000 3 2014 2019
Bronchopulmonary Dysplasia
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
112 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.020 1.000 2 2015 2015
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.020 1.000 2 2008 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.020 1.000 2 2018 2019
Hypoxic-Ischemic Encephalopathy
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
12 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.020 1.000 2 2014 2016
Low Tension Glaucoma
CUI: C0152136
Disease: Low Tension Glaucoma
56 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.020 1.000 2 2012 2017
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2019 2019
Adenocarcinoma Of Esophagus
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
81 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2011 2011
Ataxia with vitamin E deficiency
CUI: C1848533
Disease: Ataxia with vitamin E deficiency
32 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2018 2018
Azoospermia
CUI: C0004509
Disease: Azoospermia
70 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2018 2018
Borderline Personality Disorder
CUI: C0006012
Disease: Borderline Personality Disorder
82 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2015 2015
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2010 2010
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1 2019 2019
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2018 2018
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2011 2011
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2016 2016
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2016 2016
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2011 2011
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2011 2011
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2018 2018