rs5049, AGT

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 1 230714337 intron variant C/T snv 0.16 0.020 1.000 2 2011 2013
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 1.000 0.040 1 230714337 intron variant C/T snv 0.16 0.010 1.000 1 2011 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 1.000 0.040 1 230714337 intron variant C/T snv 0.16 0.010 1.000 1 2011 2011