Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 22
rs121912654 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs28934874 0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs730882025 0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs786201059 0.701 0.360 17 7673764 stop gained C/A;G;T snv 20
rs863224451 0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs587780073 0.708 0.400 17 7674262 missense variant T/C;G snv 19
rs753660142 0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs148924904 0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
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 17
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 16
rs876659802 0.732 0.440 17 7673787 missense variant G/A;C;T snv 16
rs985033810 0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs121912655 0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs587782664 0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 15
rs730882026 0.742 0.440 17 7674256 missense variant T/C;G snv 15
rs587782177 0.763 0.200 17 7674887 missense variant C/A;G;T snv 11
rs1057519988 0.776 0.240 17 7673812 missense variant A/C;G;T snv 10
rs1057519995 0.807 0.240 17 7674200 missense variant T/A snv 9
rs1057519997 0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs587782529 0.851 0.200 17 7670700 missense variant G/A;C snv 8