Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2010963
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C2676832
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1(finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1(finding) 		0.700 0
dbSNP: rs138551969
rs138551969
VEGFA
1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2018 2018
dbSNP: rs138551969
rs138551969
VEGFA
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
VEGFA
1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia 		0.700 1.000 1 2018 2018
dbSNP: rs138551969
rs138551969
VEGFA
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
VEGFA
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
VEGFA
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
VEGFA
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
VEGFA
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: rs1005230
rs1005230
VEGFA
0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		0.010 1.000 1 2018 2018
dbSNP: rs1005230
rs1005230
VEGFA
0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs1005230
rs1005230
VEGFA
0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60
CUI: C0017638
Disease: Glioma
Glioma 		0.010 1.000 1 2018 2018
dbSNP: rs1005230
rs1005230
VEGFA
0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs1005230
rs1005230
VEGFA
0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs10434
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.010 1.000 1 2018 2018
dbSNP: rs10434
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2009 2009
dbSNP: rs10434
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs10434
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0018023
Disease: Nodular Goiter
Nodular Goiter 		0.010 1.000 1 2017 2017
dbSNP: rs10434
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0344315
Disease: Depressed mood
Depressed mood 		0.010 1.000 1 2014 2014
dbSNP: rs10434
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0011570
Disease: Mental Depression
Mental Depression 		0.010 1.000 1 2014 2014
dbSNP: rs10434
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs10434
rs10434
VEGFA
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 		0.010 1.000 1 2017 2017
dbSNP: rs10434
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 1.000 1 2019 2019
dbSNP: rs10434
rs10434
VEGFA
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 		0.010 1.000 1 2009 2009
dbSNP: rs10434
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.010 1.000 1 2017 2017