Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
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 22
rs1057519997 0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
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
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
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
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs730882025 0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25
rs863224451 0.701 0.440 17 7673796 missense variant C/A;G;T snv 20