Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3731217
rs3731217
0.763 0.320 9 21984662 intron variant A/C;T snv
Childhood Acute Lymphoblastic Leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.050 1.000 5 2010 2018
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
Childhood Acute Lymphoblastic Leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.030 1.000 3 2015 2018
dbSNP: rs2811709
rs2811709
1.000 0.120 9 21980152 intron variant A/G snv 0.88
Childhood Acute Lymphoblastic Leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3731246
rs3731246
0.882 0.120 9 21971990 intron variant C/G snv 0.11
Childhood Acute Lymphoblastic Leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017