Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs138398778
ATM
1.000 0.080 11 108247071 missense variant C/A;T snv 8.0E-06; 8.8E-05 1
rs202160435
ATM
0.925 0.240 11 108247072 missense variant G/A snv 8.0E-05 6.3E-05 1
rs587779858
ATM
1.000 0.080 11 108227692 missense variant G/A snv 1
rs730881315
ATM ; C11orf65
1.000 0.080 11 108329154 stop gained C/A;T snv 4.0E-06; 8.0E-06 1
rs587782310
C11orf65 ; ATM
1.000 0.080 11 108330234 missense variant G/A snv 8.0E-06 7.0E-06 1