rs6125, SELP

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 1 169613079 missense variant C/T snv 5.6E-02 5.2E-02 0.010 1.000 1 2010 2010
Ventricular Fibrillation
CUI: C0042510
Disease: Ventricular Fibrillation
19 0.925 0.080 1 169613079 missense variant C/T snv 5.6E-02 5.2E-02 0.010 1.000 1 2010 2010