rs773371778, CETP

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.
Atherothrombosis
CUI: C1963943
Disease: Atherothrombosis
15 0.925 0.080 16 56972000 missense variant C/T snv 4.0E-06 0.010 1.000 1 2002 2002
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.925 0.080 16 56972000 missense variant C/T snv 4.0E-06 0.010 1.000 1 2002 2002