Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs121909222 0.742 0.240 10 87933127 missense variant A/G snv 13
rs767808984 0.851 0.160 14 36520098 missense variant C/G;T snv 1.3E-05 9
rs1989839 0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20 8
rs770374782 0.851 0.160 17 7673752 missense variant G/A;C snv 1.2E-05 4.2E-05 6
rs201701502 0.851 0.080 1 162775837 missense variant C/G;T snv 1.5E-04 2.1E-05 5
rs1430452530 0.851 0.160 14 61721518 missense variant A/G snv 4.0E-06 5
rs139883133 0.925 0.120 3 8548583 stop gained G/A snv 1.9E-04 6.3E-05 2
rs754533102 1.000 0.080 10 100299692 missense variant C/T snv 6.0E-05 7.0E-06 2
rs762959475 1.000 0.080 3 146124229 missense variant T/C snv 4.0E-06 1.4E-05 1