Disease: Childhood Acute Lymphoblastic Leukemia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507520
PTPN11
0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs4132601
IKZF1
0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 9
rs4748793 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 4
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs6021191
NFATC2
0.851 0.120 20 51419700 intron variant A/T snv 4.9E-02 5
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 23
rs6944602 0.925 0.120 7 50406053 downstream gene variant G/A;T snv 2
rs6964969
IKZF1
0.851 0.120 7 50405553 downstream gene variant A/G snv 0.23 4
rs7073837
ARID5B
0.851 0.120 10 61940136 intron variant A/C snv 0.58 0.64 4
rs7088318
PIP4K2A
0.851 0.120 10 22564019 intron variant C/A snv 0.55 4
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs775144154
SLC19A1
0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs924607
LOC105374608 ; LOC100996325
0.851 0.120 5 609978 intron variant C/T snv 0.32 7