Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2107357 | 16 | 27399508 | upstream gene variant | A/G | snv | 0.85 | 1 | ||||
rs2197415 | 10 | 9020893 | intergenic variant | T/G | snv | 0.66 | 1 | ||||
rs2507978 | 6 | 31383887 | upstream gene variant | G/A | snv | 0.50 | 1 | ||||
rs2589561 | 1.000 | 0.080 | 10 | 9004682 | intergenic variant | A/G | snv | 0.83 | 1 | ||
rs28895016 | 6 | 31606748 | downstream gene variant | C/T | snv | 5.4E-02 | 1 | ||||
rs343478 | 9 | 6051399 | intron variant | G/A;C | snv | 1 | |||||
rs3939286 | 0.776 | 0.360 | 9 | 6210099 | regulatory region variant | T/A;C | snv | 1 | |||
rs4090390 | 1 | 173177782 | upstream gene variant | C/A | snv | 0.29 | 1 | ||||
rs413382 | 1.000 | 0.080 | 9 | 6142948 | intergenic variant | C/A | snv | 0.81 | 1 | ||
rs4801001 | 18 | 54668944 | intergenic variant | T/C | snv | 0.62 | 1 | ||||
rs56129466 | 11 | 128288294 | intergenic variant | A/G | snv | 0.18 | 1 | ||||
rs5758343 | 22 | 41420648 | intergenic variant | A/T | snv | 0.82 | 1 | ||||
rs59593577 | 11 | 95692362 | intron variant | C/T | snv | 0.12 | 1 | ||||
rs6473223 | 8 | 80355920 | intron variant | T/A;C | snv | 1 | |||||
rs6869502 | 5 | 110830384 | intergenic variant | A/T | snv | 0.28 | 1 | ||||
rs7032572 | 9 | 6172380 | intergenic variant | A/G | snv | 0.15 | 1 | ||||
rs7127307 | 1.000 | 0.120 | 11 | 128317488 | regulatory region variant | T/C | snv | 0.47 | 1 | ||
rs7130753 | 11 | 111599843 | upstream gene variant | C/T | snv | 0.37 | 1 | ||||
rs7214661 | 17 | 45353330 | TF binding site variant | A/G | snv | 0.39 | 1 | ||||
rs7714574 | 5 | 40492553 | intron variant | C/A;G;T | snv | 1 | |||||
rs7720838 | 0.925 | 0.040 | 5 | 40486794 | intron variant | G/T | snv | 0.52 | 1 | ||
rs7741091 | 6 | 31384854 | upstream gene variant | A/G | snv | 0.36 | 1 | ||||
rs7824394 | 8 | 80380364 | intron variant | A/C;T | snv | 1 | |||||
rs7927997 | 1.000 | 0.040 | 11 | 76590331 | upstream gene variant | C/T | snv | 0.34 | 1 | ||
rs8069176 | 0.882 | 0.080 | 17 | 39900944 | downstream gene variant | G/A;T | snv | 1 |