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 | 12 | ||
rs2248462 | 0.807 | 0.240 | 6 | 31479019 | downstream gene variant | G/A | snv | 0.19 | 8 | ||
rs2395185 | 0.724 | 0.360 | 6 | 32465390 | intron variant | G/T | snv | 0.29 | 8 | ||
rs2516049 | 0.742 | 0.400 | 6 | 32602623 | intergenic variant | T/C | snv | 0.27 | 9 | ||
rs2534657 | 0.882 | 0.200 | 6 | 31504682 | intron variant | C/T | snv | 0.15 | 6 | ||
rs2763979 | 0.827 | 0.360 | 6 | 31826815 | upstream gene variant | C/T | snv | 0.45 | 3 | ||
rs3763313 | 0.807 | 0.320 | 6 | 32408694 | upstream gene variant | A/C | snv | 0.21 | 5 | ||
rs477515 | 0.790 | 0.400 | 6 | 32601914 | intergenic variant | G/A | snv | 0.27 | 7 | ||
rs4959089 | 0.925 | 0.200 | 6 | 32251948 | upstream gene variant | A/G | snv | 0.22 | 2 | ||
rs6903608 | 0.742 | 0.400 | 6 | 32460508 | intron variant | C/G;T | snv | 5 | |||
rs707928 | 0.827 | 0.320 | 6 | 31774813 | intron variant | A/G | snv | 0.47 | 4 | ||
rs7774434 | 0.807 | 0.360 | 6 | 32689801 | TF binding site variant | T/C | snv | 0.40 | 5 | ||
rs805294 | 0.882 | 0.240 | 6 | 31720440 | intron variant | A/G | snv | 0.48 | 3 | ||
rs9296015 | 0.851 | 0.280 | 6 | 32251212 | upstream gene variant | G/A | snv | 0.22 | 4 |