Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1135401784 | 0.925 | 0.120 | 3 | 149178537 | missense variant | A/G | snv | 3 | |||
| rs386134141 | 0.925 | 0.120 | 3 | 149177980 | splice acceptor variant | C/A;T | snv | 3 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1135401784 | 0.925 | 0.120 | 3 | 149178537 | missense variant | A/G | snv | 3 | |||
| rs386134141 | 0.925 | 0.120 | 3 | 149177980 | splice acceptor variant | C/A;T | snv | 3 |