| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909215 | 0.790 | 0.200 | 5 | 136060898 | missense variant | G/A | snv | 7 | |||
| rs121909216 | 0.882 | 0.200 | 5 | 136055795 | missense variant | T/G | snv | 3 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909215 | 0.790 | 0.200 | 5 | 136060898 | missense variant | G/A | snv | 7 | |||
| rs121909216 | 0.882 | 0.200 | 5 | 136055795 | missense variant | T/G | snv | 3 |