Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519709
KIT
0.925 0.080 4 54733154 missense variant GA/AT mnv 1
rs1057519906
IDH2
0.882 0.120 15 90088607 missense variant T/A;C snv 1
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 1
rs111033563
LOC108783645 ; HFE
0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 1
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 1
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 1
rs1169288572
SETD2
1.000 0.040 3 47122237 missense variant C/T snv 8.0E-06 7.0E-06 1
rs121909646
FLT3
0.882 0.120 13 28018504 missense variant T/A;G snv 1
rs121912472
INSL6 ; JAK2
0.925 0.080 9 5073742 missense variant G/C snv 1
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 1
rs121913232
FLT3
0.925 0.120 13 28018500 missense variant G/C snv 1
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 1
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 1
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 1
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 1
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 1
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 1
rs121913502
IDH2
0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 1
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 1
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 1
rs121917759
HRAS ; LRRC56
0.790 0.480 11 533466 missense variant G/A snv 1
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 1
rs137854451
ELANE
0.925 0.080 19 856000 missense variant G/A snv 1
rs1466524306
UBAC2 ; GPR183
1.000 0.040 13 99295133 missense variant G/A snv 4.0E-06 1
rs147001633
DNMT3A
0.776 0.240 2 25234373 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.2E-04 1