Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3132453 0.925 0.200 6 31636267 missense variant T/G snv 0.96 0.95 2
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs316019 0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs3134943 0.882 0.240 6 32179984 intron variant T/A;C snv 0.89 3
rs2227956 0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 12
rs3129888 0.882 0.240 6 32443949 intron variant G/A snv 0.82 0.80 4
rs3129941 0.882 0.240 6 32369909 missense variant A/G;T snv 0.81 3
rs3130617 0.925 0.200 6 31659746 missense variant C/T snv 0.79 0.74 2
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs689 0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60 9
rs3842753 1.000 0.120 11 2159830 missense variant T/G snv 0.73 0.60 1
rs6043409 1.000 0.120 20 1635560 missense variant A/G snv 0.73 0.72 2
rs222747 0.827 0.240 17 3589906 missense variant C/A;G;T snv 0.72; 4.5E-06 8
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1801262 0.882 0.120 2 181678728 missense variant T/C snv 0.70 0.68 4
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs3747517 0.732 0.360 2 162272314 missense variant T/C snv 0.68 0.68 13
rs10774671 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs5435 0.851 0.200 17 7283804 missense variant T/A;C snv 0.65 6
rs3024866 1.000 0.120 2 191058115 splice region variant G/A snv 0.64 0.56 1
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81