Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519946 0.732 0.280 19 52212729 missense variant C/G;T snv 17
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs148924904 0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 17
rs587780073 0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs866775781 0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519996 0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs121913348 0.763 0.480 7 140781617 missense variant C/A;G;T snv 16
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 16
rs942158624 0.724 0.320 17 7674948 missense variant T/A snv 16
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 15
rs1057519985 0.724 0.360 17 7673763 missense variant T/A;C;G snv 15
rs121912655 0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 15