| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12663103 | 0.851 | 0.240 | 6 | 32193547 | intron variant | T/C | snv | 6.1E-02 | 7 | ||
| rs2523535 | 0.851 | 0.200 | 6 | 31368473 | intron variant | A/G | snv | 0.32 | 7 | ||
| rs17475879 | 0.925 | 0.040 | 6 | 30396731 | regulatory region variant | C/T | snv | 5.6E-02 | 5 |