rs10251201, UMAD1

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 0.160 7 7932654 intron variant T/A;C snv 0.010 1.000 1 2017 2017
leukemia
CUI: C0023418
Disease: leukemia
144 0.851 0.160 7 7932654 intron variant T/A;C snv 0.010 1.000 1 2017 2017
Leukemogenesis
CUI: C0598766
Disease: Leukemogenesis
25 0.851 0.160 7 7932654 intron variant T/A;C snv 0.010 1.000 1 2017 2017
Monoclonal Gammopathy of Undetermined Significance
CUI: C0026470
Disease: Monoclonal Gammopathy of Undetermined Significance
20 0.851 0.160 7 7932654 intron variant T/A;C snv 0.010 1.000 1 2018 2018