Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 13
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
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
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
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
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 17
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 13
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
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs786201059 0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs863224451 0.701 0.440 17 7673796 missense variant C/A;G;T snv 19