Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111033563 0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 1
rs121913487 0.925 0.120 13 28018503 missense variant A/C;T snv 2
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 1
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 2
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 1
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 2
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 2
rs121434595 0.708 0.320 1 114716124 missense variant C/A;G;T snv 2
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 2
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 2
rs121918454 0.742 0.280 12 112450395 missense variant C/A;G;T snv 2
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 1
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 1
rs121913250 0.683 0.440 1 114716127 missense variant C/A;G;T snv 1
rs121913488 0.807 0.120 13 28018505 missense variant C/A;G;T snv 1
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 1
rs147001633 0.776 0.240 2 25234373 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.2E-04 1
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 1
rs121913502 0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 1
rs121913503 0.689 0.200 15 90088606 missense variant C/A;T snv 1
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 1
rs104894231 0.776 0.360 11 533467 missense variant C/G;T snv 1