rs755506668, ACE

N. diseases: 1
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 17 63496874 missense variant G/A;T snv 2.8E-05; 8.0E-06 0.010 1.000 1 2010 2010