Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs1059513 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
rs7192 0.827 0.200 6 32443869 missense variant T/G snv 0.64 0.61 7
rs1295686 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 7
rs324015 0.827 0.120 12 57096317 3 prime UTR variant T/C snv 0.76 5
rs1343795 0.882 0.120 17 49334880 intron variant C/A snv 0.78 5
rs976078 0.882 0.120 13 82963398 intron variant A/C snv 0.15 4
rs4572450 0.882 0.120 17 49343367 intron variant T/C snv 0.78 4
rs4896888 1.000 0.040 6 146777855 intron variant C/T snv 0.47 2
rs1036504 1.000 0.040 7 2570131 intron variant C/T snv 0.61 2
rs2917750 1.000 0.040 7 2573790 intron variant T/G snv 0.57 2
rs4235235 1.000 0.040 4 154182301 intron variant C/T snv 0.83 1
rs9325071 1.000 0.040 5 148117775 intron variant A/G snv 0.22 1