Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs786203436 0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs876660821 0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057520004 0.752 0.240 17 7674884 missense variant A/C;T snv 11
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
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
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
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
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
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
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
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25