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
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
rs624366
ATM
0.827 0.120 11 108283370 intron variant G/C snv 0.52 6
rs11212592
ATM ; C11orf65
0.882 0.080 11 108348120 intron variant A/G snv 0.16 3
rs652311
C11orf65 ; ATM
0.882 0.080 11 108369342 intron variant G/A snv 0.54 3