Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 12
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs2069514 0.807 0.160 15 74745879 upstream gene variant G/A snv 0.13 9
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs4769793 0.807 0.120 13 29985289 intergenic variant G/C snv 8
rs36115365 0.807 0.160 5 1313127 upstream gene variant G/A;C;T snv 7
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 7
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 6
rs2736108 0.807 0.160 5 1297373 upstream gene variant C/T snv 0.24 6
rs12521436 0.827 0.120 5 143438042 upstream gene variant G/A snv 0.21 5
rs1454694 0.827 0.080 4 181276794 intergenic variant T/C snv 0.20 5