Disease: Leukemia, Myelocytic, Acute
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2454206
TET2-AS1 ; TET2
0.851 0.160 4 105275794 missense variant A/G;T snv 0.30; 6.4E-06 6
rs12199222
NUP153
1.000 0.040 6 17699091 intron variant G/A;T snv 3
rs17806888
SUCLG2
1.000 0.040 3 67365898 intron variant T/C snv 9.1E-02 3
rs2597513 1.000 0.040 3 13514336 regulatory region variant C/T snv 0.88 3
rs10757022
SAXO1
1.000 0.040 9 19023615 intron variant A/G snv 0.51 2
rs563697 1.000 0.040 2 118656877 intergenic variant A/G snv 0.25 2