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: rs138398778
rs138398778
ATM
1 1.000 0.080 11 108247071 missense variant C/A;T snv 8.0E-06; 8.8E-05 0.700 0
dbSNP: rs202160435
rs202160435
ATM
2 0.925 0.240 11 108247072 missense variant G/A snv 8.0E-05 6.3E-05 0.700 0
dbSNP: rs587779858
rs587779858
ATM
1 1.000 0.080 11 108227692 missense variant G/A snv 0.700 0
dbSNP: rs587782310
rs587782310
1 1.000 0.080 11 108330234 missense variant G/A snv 8.0E-06 7.0E-06 0.700 0
dbSNP: rs587782652
rs587782652
5 0.851 0.320 11 108335105 missense variant T/C snv 3.2E-05 4.2E-05 0.700 0
dbSNP: rs730881315
rs730881315
1 1.000 0.080 11 108329154 stop gained C/A;T snv 4.0E-06; 8.0E-06 0.700 0
dbSNP: rs772821016
rs772821016
ATM
4 0.882 0.320 11 108244873 stop gained C/T snv 4.0E-06 0.700 0