rs778747981, F2R

N. diseases: 1
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.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 1.000 0.080 5 76732556 missense variant G/A snv 8.0E-06 7.0E-06 0.010 1.000 1 2002 2002