rs10821936, ARID5B

N. diseases: 11
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 Acute Lymphoblastic Leukemia
261 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.100 1.000 11 2009 2019
Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.810 1.000 5 2009 2019
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.020 1.000 2 2014 2019
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.020 1.000 2 2014 2019
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.020 1.000 2 2014 2019
MIXED LINEAGE LEUKEMIA
CUI: C3888194
Disease: MIXED LINEAGE LEUKEMIA
2 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.020 1.000 2 2013 2017
Acute Promyelocytic Leukemia
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
21 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.010 1.000 1 2019 2019
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.010 1.000 1 2017 2017
Hyperdiploid B Acute Lymphoblastic Leukemia
13 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.010 1.000 1 2009 2009
leukemia
CUI: C0023418
Disease: leukemia
144 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.010 1.000 1 2017 2017
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.700 1.000 1 2010 2010