rs1934951, CYP2C8

N. diseases: 4
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.
Bone necrosis
CUI: C0029445
Disease: Bone necrosis
5 0.925 0.160 10 95038791 intron variant C/T snv 0.24 0.700 1.000 1 2008 2008
Anemia
CUI: C0002871
Disease: Anemia
94 0.925 0.160 10 95038791 intron variant C/T snv 0.24 0.010 1.000 1 2014 2014
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.925 0.160 10 95038791 intron variant C/T snv 0.24 0.010 1.000 1 2013 2013
Neuropathy
CUI: C0442874
Disease: Neuropathy
110 0.925 0.160 10 95038791 intron variant C/T snv 0.24 0.010 1.000 1 2014 2014