Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs2305480 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs2290400 0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 5
rs393152 0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29 5
rs1864325 0.882 0.160 17 45900461 intron variant C/T snv 0.14 5
rs8070723 0.851 0.240 17 46003698 intron variant A/G snv 0.18 5
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
rs2856683 0.827 0.320 6 32687441 regulatory region variant T/A;C;G snv 0.25 4
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 4
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 4
rs12708716 0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs2305479 0.882 0.160 17 39905964 missense variant C/T snv 0.43 0.39 4
rs7219923 0.882 0.160 17 39918265 non coding transcript exon variant C/T snv 0.52 4
rs9303281 0.882 0.160 17 39917793 non coding transcript exon variant G/A snv 0.50 4
rs9303277 0.790 0.240 17 39820216 intron variant C/T snv 0.52 4
rs694739 0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 4
rs17651549 0.882 0.160 17 45983912 missense variant C/T snv 0.15 0.14 4