rs911028477, IL4R

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.
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 1.000 0.080 16 27362773 missense variant G/A snv 0.010 1.000 1 2006 2006
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 1.000 0.080 16 27362773 missense variant G/A snv 0.010 1.000 1 2006 2006