Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs2305480 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs9272346 0.790 0.320 6 32636595 intron variant G/A snv 0.54 6
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 5
rs3117098 0.851 0.280 6 32390736 non coding transcript exon variant G/A snv 0.72 4
rs3129943 0.851 0.240 6 32370918 intron variant A/G snv 0.26 4
rs3763309 0.882 0.160 6 32408196 upstream gene variant C/A;T snv 3
rs9268516 0.882 0.200 6 32411712 upstream gene variant C/T snv 0.24 3
rs987870 0.851 0.160 6 33075103 intron variant A/G snv 0.19 3
rs881375 0.925 0.160 9 120890620 intron variant T/C snv 0.68 2
rs9275698 0.925 0.160 6 32720196 downstream gene variant A/G snv 0.37 2