rs974120, None

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.
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.851 0.200 8 2789080 intron variant T/C;G snv 0.010 1.000 1 2017 2017
leukemia
CUI: C0023418
Disease: leukemia
144 0.851 0.200 8 2789080 intron variant T/C;G snv 0.010 1.000 1 2017 2017
Leukemogenesis
CUI: C0598766
Disease: Leukemogenesis
25 0.851 0.200 8 2789080 intron variant T/C;G snv 0.010 1.000 1 2017 2017
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.851 0.200 8 2789080 intron variant T/C;G snv 0.010 1.000 1 2017 2017