Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 17
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 8
rs6013897 0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23 7
rs9275319 0.807 0.200 6 32698518 intergenic variant A/G snv 0.15 6
rs9461799 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 6
rs10853728 0.851 0.160 19 39254506 downstream gene variant C/A;G;T snv 5
rs4273729 0.851 0.240 6 32710820 upstream gene variant C/A;G;T snv 5
rs1439490 0.882 0.120 22 21351147 upstream gene variant T/C snv 3
rs7248668 0.925 0.080 19 39253181 upstream gene variant G/A snv 0.16 3
rs2856723 0.925 0.120 6 32699985 intergenic variant A/G snv 0.63 2
rs2978048 1.000 0.080 8 133603893 intergenic variant T/C;G snv 5.2E-02 2
rs7262634 1.000 0.080 20 47205635 downstream gene variant T/C snv 8.6E-02 2
rs8105790 0.925 0.160 19 39241861 upstream gene variant T/C snv 0.20 2
rs9380516 0.925 0.120 6 35534425 TF binding site variant T/C snv 0.85 2
rs111511318 1.000 0.080 5 156998817 intergenic variant C/A snv 2.9E-02 1
rs116399066 1.000 0.080 1 143723149 upstream gene variant C/A;T snv 1
rs1979860 1.000 0.080 5 174586529 regulatory region variant C/T snv 1.8E-02 1
rs2492965 1.000 0.080 6 72445473 intergenic variant T/C snv 0.90 1
rs2647006 1.000 0.080 6 32692805 intergenic variant A/C;G snv 1
rs2647051 1.000 0.080 6 32703120 downstream gene variant T/C snv 0.64 1
rs59888390 1.000 0.080 8 134989069 regulatory region variant A/G snv 0.25 1