Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs280519 0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 2
rs616488 0.925 0.080 1 10506158 intron variant A/G snv 0.27 1
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 2
rs9790517 0.925 0.080 4 105163621 intron variant C/T snv 0.20 1
rs10759243 0.925 0.080 9 107543834 upstream gene variant C/A;T snv 1
rs865686 0.851 0.080 9 108126198 regulatory region variant G/A;T snv 1
rs624366
ATM
0.827 0.120 11 108283370 intron variant G/C snv 0.52 1
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 1
rs11212617 0.827 0.200 11 108412434 intron variant C/A snv 0.49 1
rs2301241
TXN
0.827 0.160 9 110257228 upstream gene variant G/A;T snv 1
rs3806933 0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40 1
rs3204953 0.882 0.160 6 111307423 missense variant C/T snv 0.10 0.10 1
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs7086803 0.763 0.160 10 112738717 intron variant G/A snv 0.20 1
rs11196172 0.708 0.200 10 112967084 intron variant G/A snv 0.13 1
rs11196174 1.000 0.080 10 112974337 intron variant A/C;G snv 1
rs11196175 0.925 0.160 10 112976855 intron variant T/C snv 0.20 1
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs7904519 0.763 0.240 10 113014168 intron variant A/G snv 0.55 2
rs7900150 0.882 0.160 10 113034064 intron variant T/A;C snv 0.54 1
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs11552449 0.925 0.080 1 113905767 missense variant C/G;T snv 0.22 0.15 1
rs1265507 0.925 0.080 12 114430333 regulatory region variant A/G snv 0.52 1
rs1292011 0.851 0.080 12 115398717 regulatory region variant A/G snv 0.43 1
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1