Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057517452
ATM
1.000 0.200 11 108293393 frameshift variant T/- delins 1
rs1057519330
ATM
1.000 0.200 11 108249059 frameshift variant G/- del 1
rs1060501528
ATM
1.000 0.200 11 108287642 stop gained G/T snv 1
rs1060501529
ATM
1.000 0.200 11 108250978 frameshift variant TT/- delins 1
rs1060501551
ATM
1.000 0.200 11 108289683 stop gained A/T snv 1
rs1060501587
ATM
1.000 0.200 11 108272808 frameshift variant ATCA/- delins 1
rs1060501600
ATM
1.000 0.200 11 108271313 frameshift variant TCAT/- delins 1
rs1060501609
ATM
1.000 0.200 11 108249078 frameshift variant GA/- delins 1
rs1060501610
ATM
1.000 0.200 11 108253830 frameshift variant -/T ins 7.0E-06 1
rs1060501627
ATM
1.000 0.200 11 108295056 stop gained C/G;T snv 1
rs1060501642
ATM
1.000 0.200 11 108244835 frameshift variant C/- del 1
rs1060501659
ATM
1.000 0.200 11 108294947 frameshift variant AAGT/- delins 1
rs1060501669
ATM
1.000 0.200 11 108301719 stop gained G/A snv 1
rs1060501670
ATM
1.000 0.200 11 108250908 frameshift variant A/- delins 1
rs1060501679
ATM
1.000 0.200 11 108268425 stop gained TAG/AA delins 1
rs1060501684
ATM
1.000 0.200 11 108247052 frameshift variant A/- delins 1
rs1060501688
ATM
1.000 0.200 11 108307960 missense variant T/G snv 1
rs1060501690
ATM
1.000 0.200 11 108244119 splice donor variant G/A snv 4.0E-06 1
rs1060501702
ATM
1.000 0.200 11 108268545 frameshift variant G/- delins 1
rs1060501706
ATM
1.000 0.200 11 108297286 splice acceptor variant G/T snv 1
rs1064792938
ATM
1.000 0.200 11 108289695 stop gained CTGT/TAAAATAAA delins 1
rs1064792940
ATM
1.000 0.200 11 108256200 splice acceptor variant GTGGTTTACTTTAAGATTA/- del 1
rs1064792998
ATM
1.000 0.200 11 108249084 frameshift variant -/T;TTT delins 1
rs1064793390
ATM
1.000 0.200 11 108293359 frameshift variant A/- delins 1
rs112805604
ATM
1.000 0.200 11 108227889 splice donor variant G/A snv 1