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.
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
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2014 2014
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2014 2014
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
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2018 2018
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2018 2018
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2018 2018
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2019 2019
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
83 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2015 2015
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
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2016 2016
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
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2015 2015
Varicosity
CUI: C0042345
Disease: Varicosity
51 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2018 2018
Colonic Neoplasms
CUI: C0009375
Disease: Colonic Neoplasms
45 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2014 2014
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
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
CUI: C1845050
Disease: PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
37 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2015 2015
Cancer of Digestive System
CUI: C0751075
Disease: Cancer of Digestive System
15 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2014 2014
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
Strawberry nevus of skin
CUI: C0206733
Disease: Strawberry nevus of skin
10 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2018 2018
Metastatic Renal Cell Cancer
CUI: C0278678
Disease: Metastatic Renal Cell Cancer
9 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2017 2017
Metastatic Renal Cell Carcinoma
CUI: C4721698
Disease: Metastatic Renal Cell Carcinoma
9 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2017 2017
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
Palmar-plantar erythrodysesthesia syndrome
CUI: C0549410
Disease: Palmar-plantar erythrodysesthesia syndrome
8 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2016 2016