Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 101 | ||
| rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 71 | ||
| rs121913273 | 0.605 | 0.440 | 3 | 179218294 | missense variant | G/A;C | snv | 44 | |||
| rs121913281 | 0.623 | 0.520 | 3 | 179234296 | missense variant | C/T | snv | 37 | |||
| rs121913286 | 0.677 | 0.280 | 3 | 179218306 | missense variant | C/A;G | snv | 23 | |||
| rs1057519927 | 0.716 | 0.240 | 3 | 179218295 | missense variant | A/C;G;T | snv | 19 | |||
| rs397517201 | 0.732 | 0.240 | 3 | 179218307 | missense variant | A/C;G;T | snv | 16 | |||
| rs587777790 | 0.732 | 0.280 | 3 | 179199690 | missense variant | G/A | snv | 14 | |||
| rs2699887 | 0.763 | 0.280 | 3 | 179148620 | intron variant | C/T | snv | 0.18 | 11 | ||
| rs17849071 | 0.776 | 0.160 | 3 | 179218439 | intron variant | T/G | snv | 7.9E-02 | 8 | ||
| rs6443624 | 0.776 | 0.200 | 3 | 179179886 | intron variant | C/A | snv | 0.30 | 8 | ||
| rs17849079 | 0.882 | 0.120 | 3 | 179234232 | synonymous variant | C/T | snv | 2.1E-02 | 1.5E-02 | 3 | |
| rs1560137609 | 0.925 | 0.080 | 3 | 179199743 | frameshift variant | -/T | delins | 2 |