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.
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 0.500 2 2014 2017
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
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
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
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
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
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
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2017 2017
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
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2016 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2016 2016
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2018 2018
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
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
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
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
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
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
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2016 2016
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
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
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
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
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2017 2017
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2019 2019