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.
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2019 2019
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
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2018 2018
Diabetic foot ulcer
CUI: C1456868
Disease: Diabetic foot ulcer
17 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2018 2018
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2018 2018
Renal carcinoma
CUI: C1378703
Disease: Renal carcinoma
21 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2018 2018
Urologic Neoplasms
CUI: C0042076
Disease: Urologic Neoplasms
4 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1 2018 2018
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: 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
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
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
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
CUI: C0005684
Disease: 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
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
Chronic liver disease
CUI: C0341439
Disease: Chronic liver disease
14 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2017 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2017 2017
Erythema Multiforme
CUI: C0014742
Disease: Erythema Multiforme
2 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2017 2017
Hepatitis, Chronic
CUI: C0019189
Disease: Hepatitis, Chronic
10 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2017 2017
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
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.050 1.000 5 2016 2018
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
Exudative age-related macular degeneration
CUI: C0271084
Disease: Exudative age-related macular degeneration
109 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2016 2016
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2016 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
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 0.010 1.000 1 2016 2016