Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs28904921
C11orf65 ; ATM
0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 12
rs1800057
ATM
0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 11
rs664677
ATM
0.807 0.160 11 108272455 intron variant C/A;T snv 0.65 8
rs664143
C11orf65 ; ATM
0.807 0.160 11 108354934 3 prime UTR variant A/G;T snv 8
rs1800054
ATM
0.827 0.080 11 108227849 missense variant C/G;T snv 7.1E-03 7
rs769142993
ATM ; C11orf65
0.851 0.280 11 108331498 missense variant G/C;T snv 2.4E-05 7.0E-06 7
rs1800056
ATM
0.882 0.120 11 108267276 missense variant T/C snv 8.7E-03 8.5E-03 6
rs624366
ATM
0.827 0.120 11 108283370 intron variant G/C snv 0.52 6
rs775248597
ATM
0.851 0.120 11 108229185 stop gained C/G;T snv 8.1E-06 5
rs587782652
ATM ; C11orf65
0.851 0.320 11 108335105 missense variant T/C snv 3.2E-05 4.2E-05 5
rs376676328
C11orf65 ; ATM
0.882 0.280 11 108353828 missense variant A/G snv 2.2E-04 1.8E-04 5
rs4986761
ATM
0.925 0.080 11 108254034 missense variant T/C snv 8.0E-03 7.7E-03 4
rs772821016
ATM
0.882 0.320 11 108244873 stop gained C/T snv 4.0E-06 4
rs587779852
C11orf65 ; ATM
0.882 0.280 11 108312424 stop gained G/T snv 4.4E-05 3.5E-05 4
rs1801673
ATM
0.882 0.120 11 108304736 missense variant A/T snv 4.9E-03 4.4E-03 3
rs2227924
ATM
0.882 0.080 11 108251865 missense variant C/G snv 3.9E-03 1.5E-02 3
rs3092856
ATM
0.882 0.120 11 108289005 missense variant C/T snv 1.2E-02 2.2E-02 3
rs376603775
ATM
0.925 0.280 11 108304801 stop gained C/A;T snv 2.0E-05 3.5E-05 3
rs730881333
ATM
0.882 0.280 11 108243994 stop gained C/A;T snv 4.1E-06; 8.1E-06 3
rs755009196
ATM ; C11orf65
0.925 0.160 11 108332024 missense variant C/G snv 1.6E-05 2.1E-05 3
rs777741666
ATM ; C11orf65
0.925 0.080 11 108327759 splice donor variant G/A;T snv 3
rs373759
C11orf65 ; ATM
0.882 0.120 11 108349930 intron variant C/T snv 0.27 3
rs1003623
ATM
0.925 0.080 11 108281855 intron variant C/G;T snv 2