Disease: Acute lymphocytic leukemia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs397507520
PTPN11
0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs387906517
ABL1
0.827 0.120 9 130862919 missense variant G/A snv 6
rs121913448
ABL1
0.827 0.120 9 130862976 missense variant G/A snv 5
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25
rs1057519773
ABL1
0.851 0.160 9 130872901 missense variant T/A;C;G snv 4
rs121913451
ABL1
0.851 0.160 9 130872903 missense variant C/A;G snv 4
rs17007695 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 4
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 10
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1142345
TPMT
0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 9
rs2036914
F11
0.882 0.160 4 186271327 intron variant T/C snv 0.57 5
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs3731217
CDKN2A
0.763 0.320 9 21984662 intron variant A/C;T snv 10
rs4748793 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 4
rs7088318
PIP4K2A
0.851 0.120 10 22564019 intron variant C/A snv 0.55 4
rs2239633
CEBPE
0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 12
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44