Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs3745274 0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs698 0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs1044396 0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs27072 0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs1137070 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs686 0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs130058 0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs1800955 0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs2279343 0.776 0.200 19 41009358 missense variant A/G snv 0.13 8
rs28399433 0.827 0.200 19 40850474 intron variant A/C;G;T snv 0.10; 4.4E-06 7
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 7
rs1329650 0.882 0.080 10 91588363 regulatory region variant G/A;T snv 6
rs588765 0.827 0.200 15 78573083 intron variant T/A;C snv 6
rs1948 0.827 0.160 15 78625057 synonymous variant A/G;T snv 0.69 5
rs2653349 0.882 0.120 6 55277539 missense variant A/G;T snv 0.84; 4.0E-06 5
rs9332377 0.882 0.120 22 19968169 intron variant C/A;T snv 5
rs660652 1.000 0.080 15 78595490 3 prime UTR variant A/G;T snv 3
rs68081839 0.882 0.080 11 105762027 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT delins 3
rs72552266 0.882 0.200 19 41089049 stop gained C/G;T snv 4.0E-06; 5.8E-03 3
rs8192789 1.000 0.080 19 41091846 missense variant C/A;T snv 4.0E-06; 3.1E-02 3
rs9217 1.000 0.080 17 7459769 3 prime UTR variant T/A;C snv 3