| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894615 | 0.925 | 0.080 | 17 | 56594838 | missense variant | G/C | snv | 2 | |||
| rs104894603 | 1.000 | 0.080 | 17 | 56594872 | missense variant | T/G | snv | 1 | |||
| rs1567745119 | 1.000 | 0.080 | 17 | 56594837 | stop gained | G/A | snv | 1 | |||
| rs387906844 | 1.000 | 0.080 | 17 | 56594919 | missense variant | C/G;T | snv | 1.1E-05 | 1 |