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: 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: C0740394
Disease: Hyperuricemia
Hyperuricemia
Pathological Conditions, Signs and Symptoms 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: 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: 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: 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: 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: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.060 0.833 6 2010 2017
dbSNP: rs833061
rs833061
0.605 0.600 6 43769749 upstream gene variant C/G;T snv
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
Eye Diseases 0.060 0.833 6 2009 2019
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
Eye Diseases 0.050 0.800 5 2009 2019
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: rs1222213359
rs1222213359
0.574 0.720 6 43770966 missense variant G/A snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.040 1.000 4 2005 2018
dbSNP: rs1413711
rs1413711
0.882 0.200 6 43772941 intron variant T/A;C snv
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
Eye Diseases 0.040 1.000 4 2012 2014
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.040 1.000 4 2015 2018
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.040 0.750 4 2005 2013
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.040 0.750 4 2013 2017
dbSNP: rs2146323
rs2146323
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.040 1.000 4 2011 2018
dbSNP: rs3025039
rs3025039
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13
CUI: C0014175
Disease: Endometriosis
Endometriosis
Female Urogenital Diseases and Pregnancy Complications 0.040 0.750 4 2008 2020
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
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
Conventional (Clear Cell) Renal Cell Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.040 0.750 4 2017 2018
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.040 0.750 4 2017 2018