VEGFA, vascular endothelial growth factor A, 7422

N. diseases: 1899; N. variants: 59
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs833069
rs833069
0.851 0.200 6 43774842 non coding transcript exon variant T/C;G snv
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
Polypoidal choroidal vasculopathy
0.020 1.000 2 2012 2015
dbSNP: rs10434
rs10434
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C1868683
Disease: B-CELL MALIGNANCY, LOW-GRADE
B-CELL MALIGNANCY, LOW-GRADE
0.010 1.000 1 2015 2015
dbSNP: rs1305315912
rs1305315912
1.000 0.080 6 43770736 synonymous variant C/T snv
CUI: C0521158
Disease: Recurrent tumor
Recurrent tumor
0.010 1.000 1 2009 2009
dbSNP: rs1346131223
rs1346131223
1.000 6 43777657 missense variant A/G snv 7.4E-06
CUI: C1853238
Disease: Conotruncal defect
Conotruncal defect
0.010 1.000 1 2017 2017
dbSNP: rs138551969
rs138551969
1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05
Creatinine measurement, serum (procedure)
0.700 1.000 1 2018 2018
dbSNP: rs138551969
rs138551969
1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2018 2018
dbSNP: rs138551969
rs138551969
1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2018 2018
dbSNP: rs1443465532
rs1443465532
0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06
CUI: C1510885
Disease: Angiogenic Switch
Angiogenic Switch
0.010 1.000 1 2002 2002
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0278678
Disease: Metastatic Renal Cell Cancer
Metastatic Renal Cell Cancer
0.010 1.000 1 2017 2017
dbSNP: rs3025021
rs3025021
0.882 0.160 6 43781426 non coding transcript exon variant T/C snv 0.70
CUI: C2697758
Disease: Interleukin 10 Measurement
Interleukin 10 Measurement
0.700 1.000 1 2017 2017
dbSNP: rs554561071
rs554561071
6 43777513 missense variant A/G snv 1.2E-05 3.5E-05
CUI: C1402294
Disease: Primary Lesion
Primary Lesion
0.010 1.000 1 2019 2019
dbSNP: rs749491856
rs749491856
1.000 6 43782071 missense variant A/C snv
CUI: C3160887
Disease: Node-positive breast cancer
Node-positive breast cancer
0.010 1.000 1 2010 2010
dbSNP: rs833070
rs833070
0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs833070
rs833070
0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2016 2016
dbSNP: rs833070
rs833070
0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs914956206
rs914956206
0.882 0.080 6 43770762 missense variant G/A;T snv
CUI: C4049272
Disease: Tumour budding
Tumour budding
0.010 1.000 1 2015 2015
dbSNP: rs914956206
rs914956206
0.882 0.080 6 43770762 missense variant G/A;T snv
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2015 2015
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1(finding)
0.700 0
dbSNP: rs10434
rs10434
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0344315
Disease: Depressed mood
Depressed mood
Behavior and Behavior Mechanisms 0.010 1.000 1 2014 2014
dbSNP: rs10434
rs10434
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0011570
Disease: Mental Depression
Mental Depression
Behavior and Behavior Mechanisms 0.010 1.000 1 2014 2014
dbSNP: rs1212415280
rs1212415280
6 43771130 missense variant G/T snv 2.1E-05
CUI: C0085281
Disease: Addictive Behavior
Addictive Behavior
Behavior and Behavior Mechanisms 0.010 1.000 1 2019 2019
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.060 0.833 6 2010 2018
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.050 0.800 5 2010 2018
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.050 1.000 5 2016 2018
dbSNP: rs3025039
rs3025039
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.040 1.000 4 2016 2018