Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 9
rs2516400 0.827 0.320 6 31513328 upstream gene variant G/A snv 0.32 8
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs41295061 0.790 0.360 10 6072697 upstream gene variant C/A snv 6.1E-02 8
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs71597855 0.807 0.240 4 53790270 intron variant G/A snv 2.5E-02 7
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 7
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
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
rs3136534 0.807 0.240 4 122448621 downstream gene variant T/G snv 0.29 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs9461799 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 6
rs2219893 0.925 0.120 6 32801886 intergenic variant T/C snv 0.33 5