| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913482 | 0.630 | 0.680 | 4 | 1801837 | missense variant | C/T | snv | 45 | |||
| rs121913485 | 0.716 | 0.400 | 4 | 1804372 | missense variant | A/G | snv | 18 | |||
| rs121913478 | 0.708 | 0.640 | 10 | 121515280 | missense variant | T/C | snv | 17 | |||
| rs121913101 | 0.882 | 0.080 | 4 | 1807260 | stop lost | T/A;C;G | snv | 3 |