rs1799983, NOS3

N. diseases: 246
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.
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
59 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2015 2017
Hyperemia
CUI: C0020452
Disease: Hyperemia
3 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2009 2014
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2006 2011
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2009 2017
Infarction, Lacunar
CUI: C0333559
Disease: Infarction, Lacunar
18 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2004 2009
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2009 2010
Low Tension Glaucoma
CUI: C0152136
Disease: Low Tension Glaucoma
56 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2012 2016
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2012 2013
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2010 2018
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 0.500 2 2007 2011
Periodontal Diseases
CUI: C0031090
Disease: Periodontal Diseases
22 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2006 2018
Respiratory Distress Syndrome, Newborn
CUI: C0035220
Disease: Respiratory Distress Syndrome, Newborn
37 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2013 2014
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2012 2017
Spina Bifida
CUI: C0080178
Disease: Spina Bifida
61 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2004 2007
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2010 2018
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2013 2018
Thromboangiitis Obliterans
CUI: C0040021
Disease: Thromboangiitis Obliterans
16 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 0.500 2 2002 2010
Vasculitis
CUI: C0042384
Disease: Vasculitis
24 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 0.500 2 2003 2015
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.020 1.000 2 2011 2016
ABLEPHARON-MACROSTOMIA SYNDROME
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
14 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009
Acute hepatitis
CUI: C0267797
Disease: Acute hepatitis
2 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2014 2014
Acute mountain sickness
CUI: C0238284
Disease: Acute mountain sickness
3 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2018 2018
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2013 2013
Aggressive periodontitis, generalized
CUI: C1719495
Disease: Aggressive periodontitis, generalized
16 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2006 2006