Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519389 0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs61755320 0.716 0.520 16 89546737 missense variant C/T snv 2.9E-03 3.5E-03 41
rs1345176461 0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06 40
rs1043679457 0.752 0.400 5 60927745 intron variant C/A;G;T snv 33
rs74315401 0.683 0.320 20 4699525 missense variant C/T snv 32
rs113994095 0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 31
rs727502818 0.790 0.160 11 17772053 missense variant G/A snv 26
rs267608327 0.763 0.200 X 154030631 splice acceptor variant CCTCGGAGCTCTCGGGCTCAGGTGGAGGTGGGGGCAGGGGT/- delins 25
rs28933385 0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 25
rs1555745467 0.752 0.240 19 13262771 missense variant C/A snv 23
rs63750231 0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs28936415 0.752 0.320 16 8811153 missense variant G/A snv 4.1E-03 3.7E-03 22
rs113994097 0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 22
rs267606670 0.790 0.320 19 41968837 missense variant C/A;T snv 19
rs387906799 0.742 0.200 2 240788118 missense variant G/A snv 19
rs606231435 0.827 0.240 19 41970539 missense variant C/T snv 18
rs181109321 0.776 0.320 8 63065904 splice region variant C/A;T snv 2.0E-05 17
rs758361736 0.776 0.240 15 89649836 missense variant T/G snv 1.3E-05 1.4E-05 16
rs1554768245 0.807 0.160 6 152472395 frameshift variant C/- delins 16
rs1057519429 0.807 0.240 19 13235666 missense variant C/G;T snv 15
rs771379232 0.790 0.120 15 79845338 stop gained G/A snv 2.0E-05 3.5E-05 15
rs74315407 0.732 0.240 20 4699848 missense variant G/A snv 8.0E-06 2.1E-05 15
rs753635972 0.790 0.120 15 79845388 missense variant C/T snv 3.2E-05 2.1E-05 15
rs121908212 0.732 0.160 19 13303877 missense variant G/A snv 14
rs1064797245 0.776 0.280 19 41970540 missense variant G/A snv 12