Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs147978363 1.000 0.080 16 22257356 missense variant C/T snv 6.7E-04 5.6E-04 1
rs555460132 1.000 0.080 7 44228798 missense variant G/A snv 1.9E-04 2.0E-04 1
rs758268804 1.000 0.080 6 3077855 missense variant G/A snv 3.2E-05 1.0E-04 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
rs373632999 1.000 0.080 7 98949733 missense variant G/A snv 1.2E-05 4.2E-05 1
rs765563230 1.000 0.080 3 131349687 missense variant G/A snv 2.0E-05 3.5E-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
rs764355898
NRK
1.000 0.080 X 105923145 missense variant A/C snv 7.9E-05 1.9E-05 1
rs539738963 1.000 0.080 1 36348807 missense variant C/T snv 2.2E-05 1.4E-05 1
rs774996232 1.000 0.080 6 3077805 missense variant C/T snv 1.6E-05 1.4E-05 1
rs1294404368 1.000 0.080 7 98981947 missense variant C/T snv 4.4E-06 1.4E-05 1
rs1262765773 1.000 0.080 12 64485493 missense variant G/A snv 7.0E-06 1
rs759012409 1.000 0.080 6 3083284 missense variant C/T snv 4.1E-06 7.0E-06 1
rs376894109 1.000 0.080 1 2175293 missense variant C/T snv 4.0E-06 7.0E-06 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
rs528967912 1.000 0.080 7 98964724 missense variant C/T snv 1.6E-05 7.0E-06 1
rs1407808379 1.000 0.080 3 49862154 missense variant G/A snv 7.0E-06 1
rs587782310 1.000 0.080 11 108330234 missense variant G/A snv 8.0E-06 7.0E-06 1
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