rs201977733, UTS2

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 1 7850908 missense variant C/T snv 5.6E-05 2.1E-05 0.010 1.000 1 2009 2009