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: rs1005230
rs1005230 		0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1005230
rs1005230 		0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1005230
rs1005230 		0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60
CUI: C0017638
Disease: Glioma
Glioma 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1005230
rs1005230 		0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1005230
rs1005230 		0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs10434
rs10434 		0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs10434
rs10434 		0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2009 2009
dbSNP: rs10434
rs10434 		0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		Neoplasms; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs10434
rs10434 		0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0018023
Disease: Nodular Goiter
Nodular Goiter 		Endocrine System Diseases 0.010 1.000 1 2017 2017
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: rs10434
rs10434 		0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs10434
rs10434 		0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2017 2017
dbSNP: rs10434
rs10434 		0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs10434
rs10434 		0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2009 2009
dbSNP: rs10434
rs10434 		0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2017 2017
dbSNP: rs10434
rs10434 		0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0038358
Disease: Gastric ulcer
Gastric ulcer 		Digestive System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs10434
rs10434 		0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10434
rs10434 		0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		Mental Disorders 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: C0013295
Disease: Duodenal Ulcer
Duodenal Ulcer 		Digestive System Diseases 0.010 1.000 1 2009 2009
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: rs10434
rs10434 		0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs1188254133
rs1188254133 		0.851 0.240 6 43781990 missense variant T/G snv 7.0E-06
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		Neoplasms 0.010 1.000 1 2002 2002
dbSNP: rs1188254133
rs1188254133 		0.851 0.240 6 43781990 missense variant T/G snv 7.0E-06
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1188254133
rs1188254133 		0.851 0.240 6 43781990 missense variant T/G snv 7.0E-06
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2002 2002