Disease: Acute lymphocytic leukemia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs1057519773
ABL1
0.851 0.160 9 130872901 missense variant T/A;C;G snv 4
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs1142345
TPMT
0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 9
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121909646
FLT3
0.882 0.120 13 28018504 missense variant T/A;G snv 3
rs121913448
ABL1
0.827 0.120 9 130862976 missense variant G/A snv 5
rs121913451
ABL1
0.851 0.160 9 130872903 missense variant C/A;G snv 4
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 25
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1339159756
INSL6 ; JAK2
0.925 0.120 9 5078395 missense variant C/G snv 2
rs17855750
IL27
0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs368087026
SLC19A1
0.637 0.520 21 45530890 missense variant G/A snv 33
rs3731217
CDKN2A
0.763 0.320 9 21984662 intron variant A/C;T snv 10
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs387906517
ABL1
0.827 0.120 9 130862919 missense variant G/A snv 6
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs397507520
PTPN11
0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49