| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1426488816 | 0.827 | 0.160 | 9 | 26913948 | splice acceptor variant | C/T | snv | 8.0E-06 | 9 | ||
| rs761885185 | 0.882 | 0.120 | 3 | 189869329 | missense variant | C/T | snv | 4.0E-06 | 3 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1426488816 | 0.827 | 0.160 | 9 | 26913948 | splice acceptor variant | C/T | snv | 8.0E-06 | 9 | ||
| rs761885185 | 0.882 | 0.120 | 3 | 189869329 | missense variant | C/T | snv | 4.0E-06 | 3 |