Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519936 0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs1057519926 0.776 0.200 3 179210293 missense variant A/T snv 10
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 20
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 23
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 17
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 20
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 7
rs121913496 0.724 0.440 11 533873 missense variant C/A;G;T snv 11
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 17
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs587782664 0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20