rs4646155, ACE2

N. diseases: 3
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 0.925 0.080 X 15579386 intron variant C/T snv 3.9E-02 0.030 1.000 3 2018 2019
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.925 0.080 X 15579386 intron variant C/T snv 3.9E-02 0.010 1.000 1 2019 2019
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.925 0.080 X 15579386 intron variant C/T snv 3.9E-02 0.010 1.000 1 2018 2018