Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519841 0.925 0.120 5 68295269 missense variant A/G snv 5
rs1057519906 0.882 0.120 15 90088607 missense variant T/A;C snv 8
rs1057519936 0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937 0.776 0.200 3 179234285 missense variant T/C snv 11
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs121913503 0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934 0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 17
rs1057519995 0.807 0.240 17 7674200 missense variant T/A snv 9
rs1057520006 0.752 0.240 17 7673799 missense variant A/C;G;T snv 14
rs121913407 0.763 0.240 3 41224645 missense variant T/C;G snv 12
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs587780071 0.732 0.240 17 7674951 missense variant G/A snv 15
rs587781991 0.724 0.240 17 7675208 missense variant C/A;T snv 17
rs587782289 0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs765848205 0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs786203436 0.701 0.280 17 7675125 missense variant A/C;G;T snv 20