Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10683701 | 1.000 | 0.120 | 12 | 57698305 | intron variant | -/ACTT | delins | 0.61 | 1 | ||
rs5844572 | 0.752 | 0.360 | 22 | 23893562 | intron variant | -/ATTC | delins | 11 | |||
rs574503121 | 1.000 | 0.120 | 6 | 33090337 | downstream gene variant | -/ATTT | delins | 4.3E-04 | 1 | ||
rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
rs373094430 | 1.000 | 0.120 | 6 | 32622847 | TF binding site variant | -/C | ins | 1 | |||
rs201386475 | 1.000 | 0.120 | 6 | 32668286 | 5 prime UTR variant | -/CA | delins | 1 | |||
rs112630268 | 1.000 | 0.120 | 13 | 113919624 | non coding transcript exon variant | -/G | ins | 1 | |||
rs11439060 | 1.000 | 0.120 | 4 | 87975555 | non coding transcript exon variant | -/G | delins | 1 | |||
rs397897657 | 1.000 | 0.120 | 21 | 44230126 | intron variant | -/G | delins | 1.7E-04 | 1 | ||
rs56323213 | 1.000 | 0.120 | 21 | 44230126 | intron variant | -/G | delins | 1 | |||
rs113652681 | 1.000 | 0.120 | 6 | 33339623 | downstream gene variant | -/G;TG | ins | 1 | |||
rs3134069 | 0.776 | 0.320 | 8 | 118952749 | upstream gene variant | A/C | snv | 9.6E-02 | 11 | ||
rs1341239 | 0.776 | 0.360 | 6 | 22303975 | intron variant | A/C | snv | 0.65 | 8 | ||
rs6457327 | 0.790 | 0.320 | 6 | 31106253 | downstream gene variant | A/C | snv | 0.66 | 7 | ||
rs6568431 | 0.790 | 0.320 | 6 | 106140931 | intron variant | A/C | snv | 0.61 | 7 | ||
rs3129878 | 0.807 | 0.360 | 6 | 32440958 | intron variant | A/C | snv | 0.30 | 6 | ||
rs729302 | 0.827 | 0.160 | 7 | 128928906 | intergenic variant | A/C | snv | 0.28 | 6 | ||
rs2844479 | 0.925 | 0.200 | 6 | 31605179 | intergenic variant | A/C | snv | 0.34 | 5 | ||
rs3129871 | 0.827 | 0.320 | 6 | 32438565 | upstream gene variant | A/C | snv | 0.59 | 5 | ||
rs6659932 | 0.827 | 0.240 | 1 | 67336688 | intron variant | A/C | snv | 0.81 | 5 | ||
rs9268644 | 0.827 | 0.360 | 6 | 32440267 | intron variant | A/C | snv | 0.68 | 5 | ||
rs11137037 | 0.851 | 0.200 | 8 | 6538661 | intron variant | A/C | snv | 0.40 | 4 | ||
rs371045754 | 0.882 | 0.200 | X | 139530726 | upstream gene variant | A/C | snv | 5.5E-06 | 1.9E-05 | 4 | |
rs9269081 | 0.851 | 0.280 | 6 | 32473323 | intron variant | A/C | snv | 0.69 | 4 | ||
rs2647046 | 0.882 | 0.200 | 6 | 32700559 | TF binding site variant | A/C | snv | 0.64 | 3 |