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.
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
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
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2014 2014
Malignant neoplasm of kidney
CUI: C0740457
Disease: Malignant neoplasm of kidney
22 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2013 2013
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2013 2013
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1 2014 2014
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2018 2018
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2015 2015
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2013 2013
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1 2014 2014
Renal carcinoma
CUI: C1378703
Disease: Renal carcinoma
21 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2013 2013
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2016 2016
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
92 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2016 2016
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
83 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 0.010 1.000 1 2018 2018