Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 22
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 21
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 15
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 14
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 14
rs80358721 0.724 0.320 13 32339320 stop gained C/A;G;R snv 4.2E-06 11
rs121913413 0.763 0.240 3 41224634 missense variant C/A;T snv 10
rs28897672 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 10
rs80356898 0.752 0.200 17 43093844 stop gained G/A;C snv 2.8E-05; 4.0E-06 9
rs118203998 0.790 0.400 16 23603471 stop gained G/C;T snv 1.6E-05; 4.0E-06 8
rs55770810 0.763 0.280 17 43063931 missense variant G/A;T snv 2.4E-05; 8.0E-06 7
rs63750695 0.851 0.280 7 5978675 frameshift variant AAGTT/- delins 6
rs28897696 0.807 0.200 17 43063903 missense variant G/A;C;T snv 2.8E-05; 4.0E-06; 2.0E-05 5
rs41293459 0.763 0.280 17 43063930 missense variant C/A;G;T snv 2.4E-05 5
rs587781803 0.851 0.200 13 32341169 frameshift variant AAGAG/- delins 5
rs80187739 0.851 0.200 17 43067608 missense variant C/A;G;T snv 1.2E-05 5
rs80357438 0.851 0.200 17 43124032 stop gained A/G;T snv 5
rs80357474 0.827 0.200 17 43049188 missense variant A/C;G;T snv 8.0E-06 5
rs80357669 0.851 0.200 17 43093074 frameshift variant G/- delins 5