rs2227721, VTN;SARM1

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 17 28370430 intron variant C/A;T snv 0.12 0.010 1.000 1 2013 2013
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.925 0.080 17 28370430 intron variant C/A;T snv 0.12 0.010 1.000 1 2013 2013