Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs764355898
NRK
1.000 0.080 X 105923145 missense variant A/C snv 7.9E-05 1.9E-05 1
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs755089893 1.000 0.080 1 36355378 missense variant A/G snv 4.0E-06; 8.0E-06 1
rs952665081 1.000 0.080 20 9580201 missense variant A/G snv 1
rs751398376 1.000 0.080 2 178609836 missense variant C/A;G snv 1.2E-05; 4.0E-06 1
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs121913361 0.807 0.280 7 140753349 missense variant C/A;G;T 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
rs730881315 1.000 0.080 11 108329154 stop gained C/A;T snv 4.0E-06; 8.0E-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
rs1207121718 1.000 0.080 12 121269557 missense variant C/T snv 1
rs1294404368 1.000 0.080 7 98981947 missense variant C/T snv 4.4E-06 1.4E-05 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
rs200709914 1.000 0.080 3 131080575 missense variant C/T snv 4.8E-05 9.8E-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
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
rs539738963 1.000 0.080 1 36348807 missense variant C/T snv 2.2E-05 1.4E-05 1
rs759012409 1.000 0.080 6 3083284 missense variant C/T snv 4.1E-06 7.0E-06 1
rs774996232 1.000 0.080 6 3077805 missense variant C/T snv 1.6E-05 1.4E-05 1