rs7177922, RYR3

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.
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.925 0.040 15 33616418 intron variant G/A snv 0.19 0.010 1.000 1 2012 2012
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.925 0.040 15 33616418 intron variant G/A snv 0.19 0.010 1.000 1 2012 2012