Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1968445 19 10568564 synonymous variant C/G;T snv 0.95 1
rs1801726 0.732 0.280 3 122284985 missense variant G/C snv 0.95 0.92 13
rs2071214 17 78223510 missense variant G/A snv 0.93 0.96 3
rs629849 0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 8
rs11515 0.882 0.040 9 21968200 3 prime UTR variant C/A;G snv 4.0E-06; 0.88 6
rs3816747 1.000 0.080 8 13499293 missense variant G/A snv 0.87 0.89 2
rs3817466 18 5410575 synonymous variant A/G snv 0.86 0.75 1
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs11203495 8 13499310 missense variant T/G snv 0.85; 4.0E-06 0.85 1
rs738792 0.827 0.240 22 23779191 missense variant C/T snv 0.84 0.80 6
rs9869263 0.925 0.080 3 190312891 synonymous variant A/C;G;T snv 8.0E-06; 0.83; 4.0E-06 3
rs471692 0.925 0.080 17 40400518 intron variant T/A;C snv 0.79 3
rs2479717 0.925 0.080 6 41937436 intron variant T/A snv 0.79 0.81 3
rs4245739 0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 19
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2227564 0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 12
rs7969931 0.851 0.080 12 25089661 missense variant C/A;G snv 1.6E-05; 0.75 5
rs1801132 0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs461155 0.925 0.120 21 38819714 synonymous variant A/G;T snv 0.72; 4.0E-06 3
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2305160 0.776 0.200 2 100974842 missense variant A/G snv 0.71 0.75 9
rs9306160 0.925 0.080 21 43687681 missense variant T/C snv 0.69 0.73 3
rs10719 0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1056719 9 87707108 missense variant G/A snv 0.67 0.59 1