rs7729269, MCC

N. diseases: 3
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.
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.925 0.040 5 113384697 intron variant T/C snv 0.17 0.010 1.000 1 2017 2017
Skin toxicity
CUI: C1167791
Disease: Skin toxicity
24 0.925 0.040 5 113384697 intron variant T/C snv 0.17 0.010 1.000 1 2017 2017
Thrombocytopenia
CUI: C0040034
Disease: Thrombocytopenia
110 0.925 0.040 5 113384697 intron variant T/C snv 0.17 0.010 1.000 1 2017 2017