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.
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
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
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
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
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
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
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
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
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
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.060 0.833 6 2010 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.050 0.800 5 2010 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.030 1.000 3 2010 2018
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2010 2010
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 1.000 2 2011 2013
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
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
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.030 1.000 3 2012 2019
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 1.000 2 2012 2018
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2012 2012
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2012 2012
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
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2012 2012
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 2 2013 2016
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 0.500 2 2013 2020
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
269 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 2 2013 2016