rs5982, F13A1

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.
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.882 0.160 6 6174633 missense variant G/A snv 0.21 0.19 0.010 1.000 1 2002 2002
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.160 6 6174633 missense variant G/A snv 0.21 0.19 0.010 1.000 1 2002 2002
Intestinal Obstruction
CUI: C0021843
Disease: Intestinal Obstruction
3 0.882 0.160 6 6174633 missense variant G/A snv 0.21 0.19 0.010 1.000 1 2018 2018