| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12203592 | 0.649 | 0.320 | 6 | 396321 | intron variant | C/T | snv | 0.10 | 38 | ||
| rs1805007 | 0.695 | 0.280 | 16 | 89919709 | missense variant | C/A;G;T | snv | 4.4E-02 | 25 | ||
| rs1042602 | 0.925 | 0.080 | 11 | 89178528 | missense variant | C/A | snv | 0.25 | 0.24 | 6 | |
| rs1057516029 | 0.882 | 0.160 | 5 | 14290809 | stop gained | G/T | snv | 6 | |||
| rs12931267 | 1.000 | 0.040 | 16 | 89752324 | intron variant | C/G | snv | 4.7E-02 | 4 | ||
| rs1560419312 | 1.000 | 0.120 | 4 | 54729344 | missense variant | T/G | snv | 4 | |||
| rs2153271 | 0.925 | 0.160 | 9 | 16864523 | intron variant | C/T | snv | 0.43 | 3 | ||
| rs367899983 | 1.000 | 0.120 | 9 | 16864524 | intron variant | GTCT/- | delins | 4.2E-05 | 2 | ||
| rs1540771 | 1.000 | 0.040 | 6 | 466033 | intron variant | C/A;T | snv | 2 | |||
| rs619865 | 1.000 | 0.040 | 20 | 35279894 | intron variant | A/G | snv | 0.94 | 0.94 | 2 |