rs2106809, ACE2

N. diseases: 8
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.
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.827 0.120 X 15599938 intron variant A/G snv 0.19 0.040 1.000 4 2014 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.827 0.120 X 15599938 intron variant A/G snv 0.19 0.020 1.000 2 2007 2016
cardiac event
CUI: C0741923
Disease: cardiac event
18 0.827 0.120 X 15599938 intron variant A/G snv 0.19 0.010 1.000 1 2013 2013
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.827 0.120 X 15599938 intron variant A/G snv 0.19 0.010 1.000 1 2018 2018
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.827 0.120 X 15599938 intron variant A/G snv 0.19 0.010 1.000 1 2008 2008
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.827 0.120 X 15599938 intron variant A/G snv 0.19 0.010 1.000 1 2013 2013
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.827 0.120 X 15599938 intron variant A/G snv 0.19 0.010 1.000 1 2019 2019
Lone atrial fibrillation
CUI: C0340489
Disease: Lone atrial fibrillation
11 0.827 0.120 X 15599938 intron variant A/G snv 0.19 0.010 1.000 1 2013 2013