rs4086116, CYP2C9

N. diseases: 1
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.
WARFARIN SENSITIVITY (disorder)
CUI: C2608079
Disease: WARFARIN SENSITIVITY (disorder)
8 10 94947445 intron variant C/T snv 0.19 0.010 1.000 1 2019 2019