Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs267607040 0.851 0.320 18 44951948 missense variant G/A snv 4
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs121913487 0.925 0.120 13 28018503 missense variant A/C;T snv 2
rs387906631 0.882 0.080 3 128481901 missense variant G/A snv 2
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 2
rs121913506
KIT
0.677 0.320 4 54733154 missense variant G/A;C;T snv 2
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 2
rs104894366 0.776 0.400 12 25245284 missense variant G/A;C snv 2
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 2
rs104894228 0.605 0.560 11 534286 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
rs121918453 0.732 0.280 12 112450394 missense variant G/A;C;T snv 2
rs121918454 0.742 0.280 12 112450395 missense variant C/A;G;T snv 2
rs397507510 0.776 0.280 12 112450361 missense variant G/A;C;T snv 2
rs569067880 0.925 0.080 4 105234864 missense variant G/A;C snv 4.0E-06; 4.0E-06 2
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs267606708
CBL
0.925 0.040 11 119278541 missense variant G/A snv 4.0E-06 2.1E-05 1
rs28931590 1.000 0.040 19 33302164 missense variant T/A snv 1
rs869312828 0.807 0.080 5 177512369 missense variant C/T snv 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