Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs4636297 0.724 0.360 9 136670698 intron variant A/G snv 0.67 0.65 14
rs2292239 0.742 0.480 12 56088396 intron variant T/G snv 0.65 13
rs7756992 0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs5742612 0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11
rs869109213 0.790 0.200 7 150997269 intron variant GGGGGTGAGGAAGTCTAGACCTGCTGCG/A delins 10
rs11196205 0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs12050217 0.827 0.160 14 96262416 intron variant A/G snv 0.21 6
rs17883901 0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02 6
rs3825932 0.827 0.360 15 78943104 intron variant T/C snv 0.50 6
rs1073203 0.882 0.160 5 125983763 intron variant C/G snv 0.15 4
rs4838605 0.882 0.160 10 48491914 intron variant C/T snv 0.38 4
rs9640883 0.882 0.120 7 134431881 intron variant G/A snv 0.21 4
rs10507875 0.925 0.160 13 77943119 intron variant A/G snv 0.17 3
rs12267418 0.882 0.280 10 19425625 intron variant G/A snv 0.18 3
rs16999051 0.882 0.280 20 17380837 intron variant C/T snv 0.13 3
rs9362054 0.882 0.160 6 84468550 intron variant T/C snv 0.52 3
rs1002630 0.925 0.160 7 29388454 intron variant G/A snv 0.16 2
rs1249719 1.000 0.120 9 114235944 intron variant G/A snv 6.8E-02 2
rs1571942 0.925 0.160 10 20253705 intron variant A/G snv 0.15 2