rs3025039, VEGFA

N. diseases: 62
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.
Early-Stage Breast Carcinoma
CUI: C2986665
Disease: Early-Stage Breast Carcinoma
7 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2013 2013
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.030 1.000 3 2014 2017
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.020 0.500 2 2014 2019
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.020 0.500 2 2014 2019
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2014 2014
Pregnancy associated hypertension
CUI: C0852036
Disease: Pregnancy associated hypertension
43 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2014 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.020 1.000 2 2015 2016
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
83 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.020 1.000 2 2015 2018
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
CUI: C1845050
Disease: PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
37 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2015 2015
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2015 2015
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.040 1.000 4 2016 2018
Asthma
CUI: C0004096
Disease: Asthma
1536 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2016 2016
Glioma
CUI: C0017638
Disease: Glioma
353 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2016 2016
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2016 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2016 2016
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2017 2017
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2017 2017
Biliary Atresia
CUI: C0005411
Disease: Biliary Atresia
32 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1 2018 2018
Congenital atresia of extrahepatic bile duct
CUI: C4520983
Disease: Congenital atresia of extrahepatic bile duct
19 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1 2018 2018
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2018 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2018 2018
Infantile hemangioma
CUI: C4317089
Disease: Infantile hemangioma
4 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2018 2018
Strawberry nevus of skin
CUI: C0206733
Disease: Strawberry nevus of skin
10 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2018 2018
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.020 1.000 2 2019 2019