Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4363
rs4363
ACE
1.000 0.080 17 63497131 splice region variant G/A;C snv 0.52
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2010 2010
dbSNP: rs4363
rs4363
ACE
1.000 0.080 17 63497131 splice region variant G/A;C snv 0.52
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2013 2013