Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.060 0.833 6 2009 2019
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.040 1.000 4 2011 2017
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.040 1.000 4 2014 2020
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.030 1.000 3 2014 2017
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.030 1.000 3 2014 2017
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.030 0.667 3 2013 2016
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.030 1.000 3 2014 2017
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.020 1.000 2 2014 2017
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.020 1.000 2 2019 2019
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.010 1.000 1 2014 2014
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2014 2014
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		0.010 1.000 1 2014 2014
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2018 2018
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0553723
Disease: Squamous cell carcinoma of skin
Squamous cell carcinoma of skin 		0.010 1.000 1 2016 2016
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0017638
Disease: Glioma
Glioma 		0.010 1.000 1 2018 2018
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2018 2018
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0848548
Disease: hypertensive nephropathy
hypertensive nephropathy 		0.010 1.000 1 2011 2011
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		0.010 1.000 1 2014 2014
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 1.000 1 2015 2015
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 < 0.001 1 2014 2014
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.010 1.000 1 2012 2012
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.010 < 0.001 1 2013 2013
dbSNP: rs833061
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C1378703
Disease: Renal carcinoma
Renal carcinoma 		0.010 1.000 1 2013 2013