Gene: ATM ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs587782292
rs587782292
ATM ; C11orf65
2 1.000 0.200 11 108365359 missense variant C/G;T snv 1.6E-05 2.1E-05 0.810 1.000 29 1995 2017
dbSNP: rs786203054
rs786203054
ATM
2 1.000 0.200 11 108271074 missense variant T/A;G snv 0.800 1.000 27 1995 2017
dbSNP: rs397514577
rs397514577
ATM ; C11orf65
4 0.882 0.280 11 108317374 missense variant C/A snv 4.0E-06 0.800 1.000 25 1995 2017
dbSNP: rs587779872
rs587779872
ATM ; C11orf65
4 1.000 0.200 11 108345818 missense variant C/T snv 3.2E-05 1.4E-05 0.800 1.000 25 1995 2017
dbSNP: rs121434216
rs121434216
ATM ; C11orf65
2 0.925 0.200 11 108345804 missense variant T/G snv 0.800 1.000 23 1995 2017
dbSNP: rs587781511
rs587781511
ATM
1 1.000 0.200 11 108247029 missense variant A/G snv 8.0E-06 7.0E-06 0.800 1.000 23 1995 2017
dbSNP: rs587782202
rs587782202
ATM ; C11orf65
2 1.000 0.200 11 108345870 missense variant G/A;C snv 2.0E-05 0.800 1.000 23 1995 2017
dbSNP: rs121434218
rs121434218
ATM ; C11orf65
2 0.925 0.200 11 108333925 missense variant T/C;G snv 0.700 1.000 22 1995 2017
dbSNP: rs1555114558
rs1555114558
ATM ; C11orf65
1 1.000 0.200 11 108317377 missense variant T/C snv 0.700 1.000 22 1995 2017
dbSNP: rs587781302
rs587781302
ATM ; C11orf65
2 1.000 0.200 11 108315863 missense variant A/G;T snv 0.800 1.000 22 1995 2017
dbSNP: rs786202826
rs786202826
ATM ; C11orf65
3 0.925 0.280 11 108353805 missense variant A/G;T snv 4.0E-06 0.800 1.000 22 1995 2017
dbSNP: rs876659365
rs876659365
ATM ; C11orf65
2 1.000 0.200 11 108330314 missense variant T/G snv 0.800 1.000 22 1995 2017
dbSNP: rs876659735
rs876659735
ATM ; C11orf65
1 1.000 0.200 11 108335063 missense variant T/G snv 7.0E-06 0.700 1.000 22 1995 2017
dbSNP: rs876660927
rs876660927
ATM ; C11orf65
1 1.000 0.200 11 108345795 missense variant G/A;C snv 0.700 1.000 22 1995 2017
dbSNP: rs587778065
rs587778065
ATM
1 1.000 0.200 11 108257583 missense variant C/T snv 1.2E-05 7.0E-06 0.700 1.000 20 1995 2017
dbSNP: rs587779844
rs587779844
ATM
2 1.000 0.200 11 108301698 missense variant C/G;T snv 1.6E-05 7.0E-06 0.700 1.000 20 1995 2017
dbSNP: rs777301065
rs777301065
ATM
1 1.000 0.200 11 108251938 missense variant T/C snv 8.0E-06 0.700 1.000 20 1995 2017
dbSNP: rs780905851
rs780905851
ATM ; C11orf65
2 1.000 0.200 11 108345889 missense variant T/A;C;G snv 8.0E-06; 4.0E-06 0.700 1.000 20 1995 2017
dbSNP: rs28904921
rs28904921
ATM ; C11orf65
12 0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 0.800 1.000 19 1996 2016
dbSNP: rs121434220
rs121434220
ATM ; C11orf65
2 1.000 0.200 11 108330233 stop gained C/T snv 4.0E-06 0.700 1.000 14 1996 2016
dbSNP: rs587781894
rs587781894
ATM ; C11orf65
4 0.882 0.360 11 108365360 missense variant G/A;C snv 8.0E-06 7.0E-06 0.700 1.000 14 1998 2013
dbSNP: rs17174393
rs17174393
ATM ; C11orf65
4 0.882 0.280 11 108353881 splice donor variant G/A;C;T snv 1.6E-05 0.700 1.000 13 1996 2014
dbSNP: rs371638537
rs371638537
ATM ; C11orf65
2 1.000 0.200 11 108335959 stop gained A/C;G;T snv 1.6E-05 0.700 1.000 13 1996 2016
dbSNP: rs1137887
rs1137887
ATM
3 0.925 0.280 11 108256340 splice region variant G/A snv 4.4E-05 2.8E-05 0.700 1.000 12 1998 2016
dbSNP: rs139770721
rs139770721
ATM ; C11orf65
3 0.925 0.280 11 108315911 missense variant G/A snv 2.8E-05 7.0E-06 0.700 1.000 12 1999 2016