Source: BEFREE

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: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.020 1.000 2 2005 2011
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis 		0.010 1.000 1 2005 2005
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		0.010 1.000 1 2006 2006
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C1845050
Disease: PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS 		0.010 1.000 1 2008 2008
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease 		0.010 1.000 1 2009 2009
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2010 2010
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0848548
Disease: hypertensive nephropathy
hypertensive nephropathy 		0.010 1.000 1 2011 2011
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5 		0.010 1.000 1 2011 2011
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		0.010 1.000 1 2011 2011
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2012 2012
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2012 2012
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth 		0.010 1.000 1 2012 2012
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0242350
Disease: Erectile dysfunction
Erectile dysfunction 		0.010 1.000 1 2013 2013
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0014175
Disease: Endometriosis
Endometriosis 		0.010 1.000 1 2013 2013
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2014 2014
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2014 2014
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.010 1.000 1 2014 2014
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2015 2015
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 1.000 1 2015 2015
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs1570360
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.010 1.000 1 2015 2015