Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs137853007 0.790 0.240 22 28725254 missense variant G/A;T snv 5.2E-05 2
rs138398778
ATM
1.000 0.080 11 108247071 missense variant C/A;T snv 8.0E-06; 8.8E-05 1
rs202160435
ATM
0.925 0.240 11 108247072 missense variant G/A snv 8.0E-05 6.3E-05 1
rs587779858
ATM
1.000 0.080 11 108227692 missense variant G/A snv 1
rs730881315 1.000 0.080 11 108329154 stop gained C/A;T snv 4.0E-06; 8.0E-06 1
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs121913361 0.807 0.280 7 140753349 missense variant C/A;G;T snv 1
rs121913370 0.763 0.360 7 140753393 missense variant T/C;G snv 1
rs587782310 1.000 0.080 11 108330234 missense variant G/A snv 8.0E-06 7.0E-06 1
rs555460132 1.000 0.080 7 44228798 missense variant G/A snv 1.9E-04 2.0E-04 1
rs1207121718 1.000 0.080 12 121269557 missense variant C/T snv 1
rs1407808379 1.000 0.080 3 49862154 missense variant G/A snv 7.0E-06 1
rs373605259 1.000 0.080 3 36737396 missense variant C/T snv 5.2E-05 2.1E-05 1
rs147978363 1.000 0.080 16 22257356 missense variant C/T snv 6.7E-04 5.6E-04 1
rs137853200 0.925 0.120 1 16129440 missense variant G/A snv 1
rs145602440
KIT
1.000 0.080 4 54733118 missense variant C/T snv 1.2E-05 7.0E-06 1
rs751005114
KIT
1.000 0.080 4 54731395 missense variant G/A snv 8.0E-06 7.0E-06 1
rs952665081 1.000 0.080 20 9580201 missense variant A/G snv 1
rs765563230 1.000 0.080 3 131349687 missense variant G/A snv 2.0E-05 3.5E-05 1
rs753665559 1.000 0.080 17 12125315 missense variant G/A snv 4.0E-06 1
rs780763668 1.000 0.080 19 45280710 missense variant C/A;T snv 4.0E-06; 8.0E-06 1
rs778726488 1.000 0.080 19 3778199 missense variant C/G;T snv 1.7E-05 1
rs140599545 1.000 0.080 3 131228602 stop gained G/A;T snv 8.0E-06 1
rs200709914 1.000 0.080 3 131080575 missense variant C/T snv 4.8E-05 9.8E-05 1