Source: ALL

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: C3149657
Disease: CORONARY ARTERY SPASM 1, SUSCEPTIBILITY TO
CORONARY ARTERY SPASM 1, SUSCEPTIBILITY TO 		0.700 0
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: 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: 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: 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: 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: 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: C0344315
Disease: Depressed mood
Depressed mood 		0.010 1.000 1 2011 2011
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth 		0.010 1.000 1 2018 2018
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C1135196
Disease: Heart Failure, Diastolic
Heart Failure, Diastolic 		0.010 1.000 1 2017 2017
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.010 1.000 1 2012 2012
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0031090
Disease: Periodontal Diseases
Periodontal Diseases 		0.010 1.000 1 2018 2018
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2018 2018
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0432365
Disease: Thalidomide embryopathy syndrome
Thalidomide embryopathy syndrome 		0.010 1.000 1 2016 2016
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
Secondary malignant neoplasm of lymph node 		0.010 1.000 1 2019 2019
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus 		0.010 1.000 1 2011 2011
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		0.010 1.000 1 2017 2017
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0004509
Disease: Azoospermia
Azoospermia 		0.010 1.000 1 2018 2018