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: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.080 0.875 8 2000 2015
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.070 0.714 7 2003 2016
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0010073
Disease: Coronary Artery Vasospasm
Coronary Artery Vasospasm 		0.060 1.000 6 1998 2011
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.060 1.000 6 2010 2018
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0013537
Disease: Eclampsia
Eclampsia 		0.060 0.833 6 2005 2019
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.060 0.833 6 2004 2019
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0004096
Disease: Asthma
Asthma 		0.060 0.667 6 2002 2012
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0852036
Disease: Pregnancy associated hypertension
Pregnancy associated hypertension 		0.060 1.000 6 2001 2016
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0085413
Disease: Polycystic Kidney, Autosomal Dominant
Polycystic Kidney, Autosomal Dominant 		0.060 1.000 6 2002 2014
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0018801
Disease: Heart failure
Heart failure 		0.060 1.000 6 2010 2018
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0028754
Disease: Obesity
Obesity 		0.060 0.833 6 2004 2017
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0021364
Disease: Male infertility
Male infertility 		0.060 0.833 6 2008 2017
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.050 0.800 5 2009 2016
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0340100
Disease: High altitude pulmonary edema
High altitude pulmonary edema 		0.050 1.000 5 2002 2013
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		0.050 0.600 5 2006 2015
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases 		0.050 0.800 5 2001 2015
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis 		0.050 0.800 5 2001 2007
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.050 1.000 5 2002 2010
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.050 0.800 5 2006 2012
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		0.040 1.000 4 2009 2015
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.040 0.750 4 2014 2019
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia 		0.040 1.000 4 2004 2013
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.040 0.750 4 2014 2019
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		0.030 1.000 3 2002 2016
dbSNP: rs1799983
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
Premature coronary artery atherosclerosis 		0.030 1.000 3 2005 2017