rs2074192, ACE2

N. diseases: 9
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 0.160 X 15564667 intron variant C/T snv 0.40 0.020 1.000 2 2018 2019
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.827 0.160 X 15564667 intron variant C/T snv 0.40 0.010 1.000 1 2019 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.827 0.160 X 15564667 intron variant C/T snv 0.40 0.010 1.000 1 2018 2018
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.827 0.160 X 15564667 intron variant C/T snv 0.40 0.010 1.000 1 2018 2018
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.827 0.160 X 15564667 intron variant C/T snv 0.40 0.010 1.000 1 2018 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.827 0.160 X 15564667 intron variant C/T snv 0.40 0.010 1.000 1 2012 2012
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.827 0.160 X 15564667 intron variant C/T snv 0.40 0.010 1.000 1 2019 2019
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.827 0.160 X 15564667 intron variant C/T snv 0.40 0.010 1.000 1 2018 2018
Pregnancy associated hypertension
CUI: C0852036
Disease: Pregnancy associated hypertension
43 0.827 0.160 X 15564667 intron variant C/T snv 0.40 0.010 1 2018 2018