rs539179964, RIMS2

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.
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.882 0.080 8 104248720 missense variant C/T snv 1.6E-05 4.2E-05 0.010 1.000 1 2000 2000
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.882 0.080 8 104248720 missense variant C/T snv 1.6E-05 4.2E-05 0.010 1.000 1 2000 2000
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.080 8 104248720 missense variant C/T snv 1.6E-05 4.2E-05 0.010 1.000 1 2004 2004