| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1331463984 | 0.701 | 0.240 | 16 | 2176350 | missense variant | G/A | snv | 33 | |||
| rs1567252467 | 1.000 | 16 | 2173504 | missense variant | A/G | snv | 1 | ||||
| rs1567252659 | 1.000 | 16 | 2173812 | missense variant | C/G;T | snv | 1 | ||||
| rs1567254067 | 1.000 | 16 | 2176103 | missense variant | A/G | snv | 1 |