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-06 101
rs1057519926 0.776 0.200 3 179210293 missense variant A/T snv 10
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs1057519924 0.807 0.200 2 177234080 missense variant C/A snv 6
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs866775781 0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs1057519920 0.790 0.160 2 177234232 missense variant C/A;G;T snv 7
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 17
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121912655 0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121912656 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 28
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913496 0.724 0.440 11 533873 missense variant C/A;G;T snv 16
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 23