Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10795791 0.925 0.200 10 6066377 upstream gene variant A/G snv 0.40 2
rs154981 0.925 0.200 6 32913216 regulatory region variant C/A;G;T snv 2
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs2027856 0.925 0.200 6 32434928 upstream gene variant G/A snv 0.18 2
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2253907 0.882 0.360 6 31369093 intron variant C/T snv 0.43 3
rs2254556 0.851 0.280 6 31374854 intron variant T/C snv 0.85 4
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2395162 0.925 0.200 6 32420003 intergenic variant G/T snv 0.13 2
rs2395173 0.882 0.240 6 32437082 upstream gene variant A/G snv 0.62 3
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs2395175 0.925 0.200 6 32437249 upstream gene variant G/A snv 0.12 2
rs2516398 0.882 0.200 6 31513749 upstream gene variant G/T snv 0.70 3
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs2596560 0.851 0.280 6 31387541 intergenic variant T/C snv 0.22 4
rs2647044 0.882 0.240 6 32700133 intergenic variant G/A snv 0.10 3
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs2844533 0.925 0.200 6 31383025 upstream gene variant G/A snv 0.74 2
rs2844635 0.882 0.200 6 31107704 downstream gene variant A/G snv 0.37 3
rs2844746 0.925 0.200 6 30371825 intergenic variant T/C snv 0.69 2
rs2856683 0.827 0.320 6 32687441 regulatory region variant T/A;C;G snv 0.25 5
rs2856705 0.882 0.200 6 32703179 downstream gene variant C/T snv 0.11 3
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs3117230 0.882 0.200 6 33107858 upstream gene variant A/G snv 0.28 3
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6