Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909646
FLT3
0.882 0.120 13 28018504 missense variant T/A;G snv 3
rs121913232
FLT3
0.925 0.120 13 28018500 missense variant G/C snv 2
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
rs121913487
FLT3
0.925 0.120 13 28018503 missense variant A/C;T snv 2
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
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv 3
rs12669559
IKZF1
1.000 0.120 7 50368079 synonymous variant T/G snv 0.35 0.32 3
rs12719019 1.000 0.120 7 50408441 downstream gene variant C/T snv 0.40 2
rs12719039
IKZF1
1.000 0.120 7 50351251 intron variant T/C snv 0.25 1
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs12786200
FAT3
1.000 0.120 11 92245852 intergenic variant C/T snv 0.22 3
rs12887958 1.000 0.120 14 23113360 downstream gene variant C/T snv 0.37 1
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
rs141708090
C3orf20
1.000 0.120 3 14761602 missense variant G/T snv 1.9E-03 5.2E-04 1
rs144104656 1.000 0.120 2 118661291 regulatory region variant A/G snv 1.1E-03 3
rs147390019
NUDT15
0.925 0.120 13 48045720 missense variant G/A snv 2.6E-03 2.2E-03 2
rs147481775
DEPDC5
1.000 0.120 22 31829377 intron variant C/A snv 6.6E-03 3
rs1478147351
SETD2
1.000 0.120 3 47101485 missense variant G/A snv 7.0E-06 1
rs149940960
GREB1
1.000 0.120 2 11641492 3 prime UTR variant T/C snv 1.0E-02 3
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37