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
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
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 7
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 7
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 6
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 6
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs1394371 0.925 0.080 15 78432127 intergenic variant C/T snv 0.22 4
rs2069852 0.925 0.080 7 22732641 downstream gene variant G/A;C snv 4
rs2746150 0.851 0.240 6 29474924 downstream gene variant C/T snv 5.3E-02 4
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 4
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 3