rs212528, ECE1

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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.925 0.040 1 21259168 intron variant T/C snv 0.12 0.020 1.000 2 2007 2014
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.925 0.040 1 21259168 intron variant T/C snv 0.12 0.010 1.000 1 2014 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.925 0.040 1 21259168 intron variant T/C snv 0.12 0.010 1.000 1 2014 2014