rs4363, ACE

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 0.080 17 63497131 splice region variant G/A;C snv 0.52 0.010 1.000 1 2013 2013
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 1.000 0.080 17 63497131 splice region variant G/A;C snv 0.52 0.010 1.000 1 2010 2010