Disease: Childhood Acute Lymphoblastic Leukemia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10235796
IKZF1
0.882 0.120 7 50394939 intron variant T/C snv 0.82 3
rs104893636
HOXD4 ; HOXD3
0.882 0.120 2 176151875 missense variant A/C;T snv 5.2E-06; 7.9E-04 3
rs1051296
SLC19A1
0.882 0.120 21 45514947 3 prime UTR variant A/C snv 0.43 0.44 3
rs10519612
IL15
0.882 0.120 4 141732548 intron variant A/C snv 0.10 3
rs1057519743
CRLF2
0.827 0.120 Y 1196852 missense variant A/C snv 6
rs1057519866
NT5C2
0.851 0.120 10 103093198 missense variant C/T snv 5
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs111978267
KCNQ1
0.882 0.120 11 2751648 intron variant C/G;T snv 2.8E-05 3
rs1169704167
ATM
0.882 0.120 11 108284370 frameshift variant -/T delins 8.0E-06 3
rs1194008138
NR3C1
0.882 0.120 5 143400121 missense variant T/C snv 4.0E-06 3
rs12402181
SGIP1 ; MIR3117
0.882 0.120 1 66628488 mature miRNA variant G/A snv 0.17 0.24 3
rs12434881
CEBPE
0.882 0.120 14 23119433 5 prime UTR variant G/A snv 0.36 3
rs12803915
NEAT1 ; MIR612
0.882 0.120 11 65444508 non coding transcript exon variant G/A snv 0.16 0.17 3
rs1296957097
CHEK2
0.882 0.120 22 28719401 missense variant A/G snv 3
rs1310678797
VDR
0.882 0.120 12 47857143 missense variant C/T snv 7.0E-06 3
rs1361742125
NR3C1
0.882 0.120 5 143399842 missense variant T/C snv 4.0E-06 7.0E-06 3
rs138047632
LOC107987304 ; SLC19A1
0.882 0.120 21 45525860 missense variant A/G snv 2.4E-03 2.2E-03 3
rs140422742
CYP3A4
0.882 0.120 7 99778046 missense variant T/C;G snv 7.6E-05 6.3E-05 3
rs1412792500
NR3C1
0.882 0.120 5 143400541 missense variant T/C snv 4.0E-06 1.4E-05 3
rs1427331568
NR3C1
0.882 0.120 5 143314010 missense variant G/C snv 3
rs143125661
TPMT
0.882 0.120 6 18149120 missense variant C/T snv 4.0E-06 7.0E-06 3
rs1482545954
NLRP2
0.882 0.120 19 54982407 missense variant C/T snv 7.0E-06 3
rs1573613
ETV6
0.882 0.120 12 11894684 3 prime UTR variant T/C snv 0.48 3
rs17007695 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 4
rs17069665
FOXO3
0.882 0.120 6 108620265 intron variant A/C;G snv 4