rs568401628, ACE

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 0.882 0.120 17 63497280 missense variant C/T snv 4.5E-05 7.0E-06 0.020 1.000 2 1999 2004
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.882 0.120 17 63497280 missense variant C/T snv 4.5E-05 7.0E-06 0.010 1.000 1 1999 1999
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.882 0.120 17 63497280 missense variant C/T snv 4.5E-05 7.0E-06 0.010 1.000 1 2004 2004
Obesity
CUI: C0028754
Disease: Obesity
1111 0.882 0.120 17 63497280 missense variant C/T snv 4.5E-05 7.0E-06 0.010 1.000 1 2004 2004