Disease: leukemia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs1057519766
FLT3
0.851 0.080 13 28028203 missense variant G/C;T snv 5
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 12
rs121913521
KIT
0.790 0.120 4 54727447 missense variant T/A;C;G snv 12
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs1408538785
DNAH8
0.827 0.080 6 38761760 missense variant A/G snv 7.0E-06 6
rs1470755915
RUNX1T1
0.776 0.240 8 92005229 missense variant C/A snv 7.0E-06 10
rs1482518887
RUNX1
0.790 0.040 21 34887018 missense variant C/T snv 7.0E-06 8
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs2293157
STAT5A
0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs727503094
LRRC56 ; HRAS
0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs74315450
RUNX1
0.851 0.120 21 34859485 missense variant C/T snv 5
rs796065343
CSF3R
0.776 0.080 1 36467833 missense variant G/A snv 12
rs869312828
DDX41 ; DOK3
0.807 0.080 5 177512369 missense variant C/T snv 7
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3745274
CYP2B6
0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30