rs1353342, PCSK5

N. diseases: 2
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.
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.925 0.080 9 76259853 intron variant A/C snv 0.79 0.010 1.000 1 2011 2011
Ventricular Fibrillation
CUI: C0042510
Disease: Ventricular Fibrillation
19 0.925 0.080 9 76259853 intron variant A/C snv 0.79 0.010 1.000 1 2011 2011