rs3789679, AGT

N. diseases: 4
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 0.925 0.120 1 230713948 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.925 0.120 1 230713948 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Obesity
CUI: C0028754
Disease: Obesity
1111 0.925 0.120 1 230713948 intron variant G/A;T snv 0.010 1.000 1 2013 2013
Virus Diseases
CUI: C0042769
Disease: Virus Diseases
42 0.925 0.120 1 230713948 intron variant G/A;T snv 0.010 1.000 1 2013 2013