rs699947, VEGFA

N. diseases: 67
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.
Erythema Multiforme
CUI: C0014742
Disease: Erythema Multiforme
2 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2017 2017
Severe nonproliferative diabetic retinopathy
CUI: C0730278
Disease: Severe nonproliferative diabetic retinopathy
3 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2009 2009
Urologic Neoplasms
CUI: C0042076
Disease: Urologic Neoplasms
4 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1 2018 2018
hypertensive nephropathy
CUI: C0848548
Disease: hypertensive nephropathy
8 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2011 2011
Hepatitis, Chronic
CUI: C0019189
Disease: Hepatitis, Chronic
10 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2017 2017
Chronic liver disease
CUI: C0341439
Disease: Chronic liver disease
14 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2017 2017
Diabetic foot ulcer
CUI: C1456868
Disease: Diabetic foot ulcer
17 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2018 2018
Renal carcinoma
CUI: C1378703
Disease: Renal carcinoma
21 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2018 2018
Erectile dysfunction
CUI: C0242350
Disease: Erectile dysfunction
44 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2013 2013
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 1.000 2 2007 2010
Fever
CUI: C0015967
Disease: Fever
66 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2011 2011
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
80 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2009 2009
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
83 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2015 2015
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2012 2012
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2007 2007
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2018 2018
Exudative age-related macular degeneration
CUI: C0271084
Disease: Exudative age-related macular degeneration
109 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2016 2016
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2009 2009
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2007 2007
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2007 2007
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2014 2014
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2014 2014
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2014 2014
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2007 2007
Mucocutaneous Lymph Node Syndrome
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
195 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2006 2006