Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs186507655 0.708 0.280 1 1351675 upstream gene variant G/A snv 6.8E-03 17
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 9
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 9
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 7
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 7
rs17650792 0.827 0.080 3 49352817 downstream gene variant A/G snv 0.42 6
rs2410373 0.851 0.120 8 16066997 intergenic variant A/C snv 0.34 6
rs3136534 0.807 0.240 4 122448621 downstream gene variant T/G snv 0.29 6
rs9325782 0.851 0.120 8 16232964 intron variant C/T snv 0.87 6
rs3129859 0.827 0.320 6 32433162 intergenic variant G/C;T snv 5