rs879922, ACE2

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.
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.882 0.160 X 15572684 intron variant C/G snv 0.030 1.000 3 2018 2019
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.882 0.160 X 15572684 intron variant C/G snv 0.020 1.000 2 2018 2018
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.882 0.160 X 15572684 intron variant C/G snv 0.010 1.000 1 2018 2018
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.882 0.160 X 15572684 intron variant C/G snv 0.010 1.000 1 2018 2018