Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs36115365 0.807 0.160 5 1313127 upstream gene variant G/A;C;T snv 7
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1225976306 0.807 0.160 7 140924673 missense variant C/T snv 9.3E-06 8
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs3731249 0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 23
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs2036534 0.827 0.080 15 78534606 3 prime UTR variant T/C snv 0.26 8
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144