Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs1057519766
FLT3
0.851 0.080 13 28028203 missense variant G/C;T snv 5
rs35602083
FLT3
0.851 0.040 13 28049450 missense variant C/T snv 1.7E-02 1.6E-02 4
rs121909646
FLT3
0.882 0.120 13 28018504 missense variant T/A;G snv 3
rs1057520026
FLT3
0.925 0.040 13 28028244 missense variant T/G snv 2
rs121913232
FLT3
0.925 0.120 13 28018500 missense variant G/C snv 2
rs121913487
FLT3
0.925 0.120 13 28018503 missense variant A/C;T snv 2
rs1057519726
FLT3
1.000 0.040 13 28018502 missense variant T/A;C;G snv 1
rs1057519762
FLT3
1.000 0.040 13 28018484 missense variant A/G snv 1
rs1057519763
FLT3
1.000 0.040 13 28018504 missense variant TC/AA mnv 1
rs1057519764
FLT3
1.000 0.040 13 28027222 missense variant A/C;T snv 1
rs1057519765
FLT3
1.000 0.040 13 28027236 missense variant T/A;C snv 4.0E-06 1
rs1057519767
FLT3
1.000 0.040 13 28028205 missense variant T/C snv 1
rs1057519768
FLT3
1.000 0.040 13 28028279 missense variant T/C snv 1
rs1057519769
FLT3
1.000 0.040 13 28033974 missense variant C/A snv 1
rs1057520021
FLT3
1.000 0.040 13 28034139 missense variant A/C;G snv 4.0E-06 1
rs1057520022
FLT3
1.000 0.040 13 28034183 missense variant A/G snv 4.0E-06 1
rs1057520023
FLT3
1.000 0.040 13 28018501 missense variant A/C snv 1
rs1057520024
FLT3
1.000 0.040 13 28034147 missense variant T/C snv 4.0E-06; 4.0E-06 1
rs1057520025
FLT3
1.000 0.040 13 28034144 missense variant A/G snv 1
rs1057520043
FLT3
1.000 0.040 13 28034148 missense variant A/C snv 1
rs121913486
FLT3
1.000 0.040 13 28018503 inframe deletion ATC/- del 1
rs121913490
FLT3
1.000 0.040 13 28018498 inframe deletion GAT/- delins 1
rs121913491
FLT3
1.000 0.040 13 28034204 missense variant T/C snv 2.0E-05 7.0E-06 1
rs1244282842
FLT3
1.000 0.040 13 28052566 missense variant A/G snv 1