rs11122577, AGT

N. diseases: 2
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 0.120 1 230711810 intron variant C/A snv 0.19 0.010 1.000 1 2016 2016
Polycystic Kidney, Autosomal Dominant
35 1.000 0.120 1 230711810 intron variant C/A snv 0.19 0.010 1.000 1 2016 2016