| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
| rs1537372 | 0.752 | 0.120 | 9 | 22103184 | intron variant | G/A;T | snv | 14 | |||
| rs1412834 | 0.790 | 0.080 | 9 | 22110132 | intron variant | T/C | snv | 0.64 | 11 |