rs4407312, CST2

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 20 23826391 intron variant A/C;G;T snv 0.76; 4.1E-06; 6.6E-05 0.700 1.000 1 2011 2011