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
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs1207121718 1.000 0.080 12 121269557 missense variant C/T snv 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
rs1262765773 1.000 0.080 12 64485493 missense variant G/A snv 7.0E-06 1
rs1294404368 1.000 0.080 7 98981947 missense variant C/T snv 4.4E-06 1.4E-05 1
rs137853200 0.925 0.120 1 16129440 missense variant G/A snv 1
rs138398778
ATM
1.000 0.080 11 108247071 missense variant C/A;T snv 8.0E-06; 8.8E-05 1
rs140213020 1.000 0.080 9 91724870 missense variant C/A;T snv 8.2E-06; 2.0E-05 1
rs140599545 1.000 0.080 3 131228602 stop gained G/A;T snv 8.0E-06 1
rs1407808379 1.000 0.080 3 49862154 missense variant G/A snv 7.0E-06 1
rs145602440
KIT
1.000 0.080 4 54733118 missense variant C/T snv 1.2E-05 7.0E-06 1
rs147978363 1.000 0.080 16 22257356 missense variant C/T snv 6.7E-04 5.6E-04 1
rs149061352
TTN
1.000 0.080 2 178785717 missense variant G/A;T snv 4.4E-05; 4.0E-06 1
rs149403911
RET
1.000 0.080 10 43102492 missense variant G/A;T snv 2.0E-05 1
rs200709914 1.000 0.080 3 131080575 missense variant C/T snv 4.8E-05 9.8E-05 1
rs202160435
ATM
0.925 0.240 11 108247072 missense variant G/A snv 8.0E-05 6.3E-05 1
rs368370244 1.000 0.080 7 56087718 missense variant C/T snv 3.6E-05 5.6E-05 1
rs373605259 1.000 0.080 3 36737396 missense variant C/T snv 5.2E-05 2.1E-05 1
rs373632999 1.000 0.080 7 98949733 missense variant G/A snv 1.2E-05 4.2E-05 1
rs376029388 1.000 0.080 6 166412769 missense variant C/T snv 1.3E-05 2.1E-05 1
rs376894109 1.000 0.080 1 2175293 missense variant C/T snv 4.0E-06 7.0E-06 1
rs528967912 1.000 0.080 7 98964724 missense variant C/T snv 1.6E-05 7.0E-06 1