Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267606708
CBL
0.925 0.040 11 119278541 missense variant G/A snv 4.0E-06 2.1E-05 1
rs28931590
CEBPA ; CEBPA-DT
1.000 0.040 19 33302164 missense variant T/A snv 1
rs869312828
DDX41 ; DOK3
0.807 0.080 5 177512369 missense variant C/T snv 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
rs377577594
DNMT3A
0.827 0.240 2 25234374 missense variant G/A;C;T snv 1.2E-04; 8.0E-06 1
rs137854451
ELANE
0.925 0.080 19 856000 missense variant G/A snv 1
rs57246956
ELANE
0.882 0.080 19 855649 missense variant G/A;T snv 1
rs121913487
FLT3
0.925 0.120 13 28018503 missense variant A/C;T snv 2
rs121909646
FLT3
0.882 0.120 13 28018504 missense variant T/A;G snv 1
rs121913232
FLT3
0.925 0.120 13 28018500 missense variant G/C snv 1
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 1
rs387906631
GATA2
0.882 0.080 3 128481901 missense variant G/A snv 2
rs387906629
GATA2
0.925 0.080 3 128481270 missense variant G/A snv 1
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 1
rs121917759
HRAS ; LRRC56
0.790 0.480 11 533466 missense variant G/A snv 1
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 2
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 1
rs1057519906
IDH2
0.882 0.120 15 90088607 missense variant T/A;C snv 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
rs267606870
IDH2
0.763 0.280 15 90088703 missense variant G/A;C snv 1
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs121912472
INSL6 ; JAK2
0.925 0.080 9 5073742 missense variant G/C snv 1
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 1