rs699947, VEGFA

N. diseases: 67
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.
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.060 0.833 6 2010 2017
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.040 0.750 4 2017 2018
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 1.000 2 2015 2015
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2012 2012
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 1.000 2 2015 2015
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
269 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 2 2013 2016
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 0.500 2 2013 2020
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.030 0.667 3 2017 2019
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 1.000 2 2015 2015
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.040 0.750 4 2017 2018
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.030 0.667 3 2017 2019
Malignant neoplasm of urinary bladder
316 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.030 0.667 3 2017 2019
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2012 2012
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2019 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.030 1.000 3 2010 2018
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 1.000 2 2012 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2012 2012
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 2 2013 2016
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2016 2016
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 0.500 2 2014 2017
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2016 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2017 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 1.000 2 2017 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.020 1.000 2 2014 2014