rs35697037, BMX;ACE2

N. diseases: 2
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.
Dizziness
CUI: C0012833
Disease: Dizziness
14 X 15523993 intron variant G/A snv 0.37 0.010 1.000 1 2014 2014
Vertigo
CUI: C0042571
Disease: Vertigo
35 X 15523993 intron variant G/A snv 0.37 0.010 1.000 1 2014 2014