rs6632677, 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.
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.851 0.120 X 15596749 intron variant G/C snv 5.0E-03 0.010 1.000 1 2017 2017
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.851 0.120 X 15596749 intron variant G/C snv 5.0E-03 0.010 1 2018 2018
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.851 0.120 X 15596749 intron variant G/C snv 5.0E-03 0.010 1.000 1 2008 2008
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.851 0.120 X 15596749 intron variant G/C snv 5.0E-03 0.010 1 2018 2018