rs2010963, VEGFA

N. diseases: 82
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.
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1(finding)
CUI: C2676832
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1(finding)
1 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.700 0
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2004 2004
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.040 0.750 4 2005 2013
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2005 2005
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
59 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2006 2006
Mucocutaneous Lymph Node Syndrome
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
195 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2006 2006
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.050 0.800 5 2009 2019
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2009 2009
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
80 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2009 2009
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.060 0.833 6 2010 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.030 1.000 3 2010 2018
Glioma
CUI: C0017638
Disease: Glioma
353 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.030 1.000 3 2011 2018
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2012 2012
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2012 2012
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2012 2012
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2012 2012
Myopia
CUI: C0027092
Disease: Myopia
167 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2012 2012
Pneumonitis
CUI: C3714636
Disease: Pneumonitis
13 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2012 2012
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.040 0.750 4 2013 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.030 1.000 3 2013 2019
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1 2013 2013
Erectile dysfunction
CUI: C0242350
Disease: Erectile dysfunction
44 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2013 2013
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2013 2013
Recurrent depressive disorder
CUI: C0349218
Disease: Recurrent depressive disorder
9 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2013 2013
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.030 0.667 3 2014 2017