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.
Acute mountain sickness
CUI: C0238284
Disease: Acute mountain sickness
3 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2012 2012
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
Iodine deficiency syndrome
CUI: C0342199
Disease: Iodine deficiency syndrome
4 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2020 2020
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
Gastric ulcer
CUI: C0038358
Disease: Gastric ulcer
7 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2009 2009
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
Nodular Goiter
CUI: C0018023
Disease: Nodular Goiter
12 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2020 2020
Pneumonitis
CUI: C3714636
Disease: Pneumonitis
13 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2012 2012
ABLEPHARON-MACROSTOMIA SYNDROME
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
14 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2011 2011
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
Dystrophia myotonica 2
CUI: C2931689
Disease: Dystrophia myotonica 2
21 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2019 2019
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2011 2011
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
Duodenal Ulcer
CUI: C0013295
Disease: Duodenal Ulcer
33 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2009 2009
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
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
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
Peripheral Nervous System Diseases
CUI: C4721453
Disease: Peripheral Nervous System Diseases
69 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2019 2019
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
81 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2019 2019
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
Neuropathy
CUI: C0442874
Disease: Neuropathy
110 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2019 2019
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2009 2009
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.010 1.000 1 2012 2012
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.030 1.000 3 2012 2013
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 0.030 1.000 3 2012 2013