Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10932029 0.827 0.200 2 203937045 intron variant T/A;C snv 5
rs16851720 0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs2596538 0.851 0.160 6 31400855 intron variant G/A snv 0.41 5
rs2645424 0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs5743314 0.851 0.160 4 186079221 intron variant G/C;T snv 5
rs5998152 0.827 0.160 22 31867176 intron variant T/C snv 0.37 5
rs843645 0.827 0.120 2 54247527 intron variant T/A;G snv 0.19 5
rs10433937 0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs4656942 0.851 0.160 1 160861258 intron variant G/A;C;T snv 4
rs6715787 0.851 0.200 2 46349033 intron variant C/G;T snv 4
rs7254880 0.882 0.160 19 9298599 intron variant C/G snv 0.16 4
rs10945859 0.882 0.120 6 162721570 intron variant T/C snv 0.17 3
rs1358379 0.882 0.160 6 71403739 intron variant T/C snv 6.2E-02 3
rs1485766 0.882 0.120 4 176689730 intron variant T/A;G snv 3
rs26907 0.882 0.240 5 81069496 intron variant G/A;T snv 3
rs2843403 0.882 0.200 1 2597658 intron variant T/C snv 0.54 3
rs3820998 0.882 0.120 2 161138615 intron variant C/A;T snv 3
rs7536540 0.882 0.160 1 65058899 intron variant C/G;T snv 0.65 3
rs12104272 0.925 0.080 19 49644795 intron variant G/A snv 0.44 2
rs1227756 0.925 0.080 10 69828748 intron variant G/A;C snv 2
rs2629751 0.925 0.120 12 104028030 intron variant A/G snv 0.36 2
rs2679757 0.925 0.080 8 102858590 intron variant A/G snv 0.37 2
rs2710833 0.925 0.080 4 168488807 intron variant T/A;C snv 2
rs4646038 0.925 0.080 1 15506705 intron variant C/T snv 7.0E-06 2
rs642588 0.925 0.120 6 159990235 intron variant A/G snv 0.83 2