rs7115578, MAML2

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.
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
59 0.882 0.040 11 96266936 intron variant G/A snv 0.37 0.010 1.000 1 2019 2019
Childhood Astrocytoma
CUI: C4086152
Disease: Childhood Astrocytoma
39 0.882 0.040 11 96266936 intron variant G/A snv 0.37 0.010 1.000 1 2019 2019
Glioma
CUI: C0017638
Disease: Glioma
353 0.882 0.040 11 96266936 intron variant G/A snv 0.37 0.010 1.000 1 2019 2019