Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs186507655 0.708 0.280 1 1351675 upstream gene variant G/A snv 6.8E-03 17
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs212091 0.827 0.120 16 16142793 3 prime UTR variant T/A;C snv 5
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs2240308 0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs9915936 0.827 0.120 17 65537671 synonymous variant T/C snv 0.90 0.90 5
rs4808075 0.701 0.280 19 17279482 intron variant T/C snv 0.26 18
rs2239680 0.827 0.120 17 78223702 3 prime UTR variant T/C snv 0.27 0.24 5
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs11571818 0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 17
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43