Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10923931 | 0.925 | 0.120 | 1 | 119975336 | intron variant | G/T | snv | 0.17 | 2 | ||
rs1111875 | 0.776 | 0.360 | 10 | 92703125 | intergenic variant | C/T | snv | 0.36 | 2 | ||
rs1153188 | 0.925 | 0.120 | 12 | 54705212 | intergenic variant | T/A | snv | 0.76 | 2 | ||
rs12779790 | 0.882 | 0.120 | 10 | 12286011 | intergenic variant | A/G | snv | 0.17 | 2 | ||
rs17036101 | 0.925 | 0.120 | 3 | 12236345 | regulatory region variant | G/A;T | snv | 2 | |||
rs2237897 | 0.882 | 0.200 | 11 | 2837316 | intron variant | C/T | snv | 8.1E-02 | 2 | ||
rs2383208 | 0.882 | 0.120 | 9 | 22132077 | downstream gene variant | A/G;T | snv | 0.18 | 2 | ||
rs4607103 | 0.882 | 0.120 | 3 | 64726228 | intron variant | C/T | snv | 0.28 | 2 | ||
rs4712524 | 0.925 | 0.120 | 6 | 20657634 | intron variant | A/G | snv | 0.40 | 2 | ||
rs5015480 | 0.851 | 0.120 | 10 | 92705802 | downstream gene variant | C/T | snv | 0.42 | 2 | ||
rs5215 | 0.827 | 0.160 | 11 | 17387083 | missense variant | C/T | snv | 0.64 | 0.71 | 2 | |
rs5219 | 0.701 | 0.360 | 11 | 17388025 | stop gained | T/A;C | snv | 0.64 | 2 | ||
rs6769511 | 0.925 | 0.120 | 3 | 185812502 | intron variant | T/C | snv | 0.46 | 2 | ||
rs7020996 | 0.925 | 0.120 | 9 | 22129580 | downstream gene variant | C/A;T | snv | 2 | |||
rs7578597 | 0.807 | 0.240 | 2 | 43505684 | missense variant | T/C | snv | 9.9E-02 | 0.14 | 2 | |
rs7901695 | 0.851 | 0.160 | 10 | 112994329 | intron variant | T/C | snv | 0.34 | 2 | ||
rs7961581 | 0.827 | 0.200 | 12 | 71269322 | intron variant | C/T | snv | 0.75 | 2 | ||
rs10946398 | 0.827 | 0.160 | 6 | 20660803 | intron variant | A/C | snv | 0.40 | 3 | ||
rs12518099 | 0.925 | 0.120 | 5 | 90250292 | intron variant | A/G;T | snv | 3 | |||
rs13266634 | 0.724 | 0.480 | 8 | 117172544 | missense variant | C/A;T | snv | 0.29 | 3 | ||
rs2943641 | 0.763 | 0.160 | 2 | 226229029 | intergenic variant | T/C | snv | 0.67 | 3 | ||
rs4689388 | 0.882 | 0.360 | 4 | 6268329 | upstream gene variant | G/A | snv | 0.64 | 3 | ||
rs4712523 | 0.925 | 0.120 | 6 | 20657333 | intron variant | A/G | snv | 0.41 | 3 | ||
rs6931514 | 0.925 | 0.120 | 6 | 20703721 | intron variant | A/G | snv | 0.27 | 3 | ||
rs7754840 | 0.807 | 0.200 | 6 | 20661019 | intron variant | G/A;C;T | snv | 3 |