| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs879253887 | 0.925 | 0.120 | 11 | 68934542 | missense variant | C/T | snv | 4.1E-06 | 6 | ||
| rs1160978570 | 0.925 | 0.120 | 11 | 68933482 | splice donor variant | G/C;T | snv | 4.1E-06 | 5 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs879253887 | 0.925 | 0.120 | 11 | 68934542 | missense variant | C/T | snv | 4.1E-06 | 6 | ||
| rs1160978570 | 0.925 | 0.120 | 11 | 68933482 | splice donor variant | G/C;T | snv | 4.1E-06 | 5 |