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.
Precursor Cell Lymphoblastic Leukemia Lymphoma
126 0.756 0.143 14 23119848 regulatory region variant G/A snp 0.39 0.800 3 2009 2018
Precursor B-cell lymphoblastic leukemia
18 0.756 0.143 14 23119848 regulatory region variant G/A snp 0.39 0.700 1 2014 2014
Nasopharyngeal Neoplasms
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
183 0.756 0.143 14 23119848 regulatory region variant G/A snp 0.39 0.700 1 2010 2010
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
419 0.756 0.143 14 23119848 regulatory region variant G/A snp 0.39 0.700 1 2017 2017
Eosinophil count result
CUI: C0750879
Disease: Eosinophil count result
419 0.756 0.143 14 23119848 regulatory region variant G/A snp 0.39 0.700 1 2017 2017
Childhood Acute Lymphoblastic Leukemia
97 0.756 0.143 14 23119848 regulatory region variant G/A snp 0.39 0.020 1.000 2 2009 2015
Hyperdiploid B Acute Lymphoblastic Leukemia
10 0.756 0.143 14 23119848 regulatory region variant G/A snp 0.39 0.020 1.000 2 2015 2016
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
99 0.756 0.143 14 23119848 regulatory region variant G/A snp 0.39 0.020 1.000 2 2014 2015
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
7 0.756 0.143 14 23119848 regulatory region variant G/A snp 0.39 0.010 1 2016 2016
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
26 0.756 0.143 14 23119848 regulatory region variant G/A snp 0.39 0.010 1.000 1 2016 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
215 0.756 0.143 14 23119848 regulatory region variant G/A snp 0.39 0.010 1.000 1 2014 2014
Childhood B Acute Lymphoblastic Leukemia
1 0.756 0.143 14 23119848 regulatory region variant G/A snp 0.39 0.010 1.000 1 2016 2016