rs833061, VEGFA

N. diseases: 42
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.
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2016 2016
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2018 2018
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.060 0.833 6 2009 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2014 2014
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.030 1.000 3 2014 2017
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2015 2015
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2015 2015
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2018 2018
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2014 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.020 1.000 2 2014 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2018 2018
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2014 2014
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.040 1.000 4 2011 2017
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1 2013 2013
Exudative age-related macular degeneration
CUI: C0271084
Disease: Exudative age-related macular degeneration
109 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2017 2017
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2018 2018
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2018 2018
Glioma
CUI: C0017638
Disease: Glioma
353 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2018 2018
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
269 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1 2013 2013
hypertensive nephropathy
CUI: C0848548
Disease: hypertensive nephropathy
8 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2011 2011
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2012 2012
Idiopathic pulmonary arterial hypertension
CUI: C3203102
Disease: Idiopathic pulmonary arterial hypertension
24 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2017 2017
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2014 2014
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2013 2013
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2013 2013