| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1045118320 | 0.925 | 9 | 128332219 | missense variant | C/A | snv | 7.0E-06 | 3 | |||
| rs758522459 | 0.925 | 9 | 128323147 | missense variant | G/C | snv | 4.3E-05 | 7.0E-05 | 3 | ||
| rs141303335 | 1.000 | 9 | 128325777 | splice acceptor variant | A/G | snv | 8.0E-06 | 1.4E-05 | 1 | ||
| rs747779231 | 1.000 | 9 | 128325882 | splice donor variant | G/A;C;T | snv | 4.0E-05; 2.8E-05 | 1 | |||
| rs786204771 | 1.000 | 9 | 128332268 | inframe deletion | CCA/- | delins | 1 | ||||
| rs774395996 | 1.000 | 9 | 128332183 | missense variant | C/G;T | snv | 4.6E-06; 9.3E-06 | 1 | |||
| rs143441644 | 1.000 | 9 | 128333565 | missense variant | C/T | snv | 4.0E-06; 2.0E-04 | 1.7E-04 | 1 | ||
| rs1163170578 | 1.000 | 9 | 128332187 | missense variant | T/G | snv | 4.4E-06 | 1 | |||
| rs775607037 | 1.000 | 9 | 128332171 | stop gained | C/A;T | snv | 1.5E-05; 5.1E-06 | 1 | |||
| rs786204770 | 1.000 | 9 | 128323100 | missense variant | T/C | snv | 1 | ||||
| rs767839639 | 1.000 | 9 | 128322930 | splice donor variant | C/A;G | snv | 4.5E-06; 5.4E-05 | 1 | |||
| rs886040973 | 1.000 | 9 | 128323142 | missense variant | GC/AA | mnv | 1 | ||||
| rs766317663 | 1.000 | 9 | 128323135 | missense variant | C/T | snv | 1.3E-05 | 7.0E-06 | 1 | ||
| rs1554796655 | 1.000 | 9 | 128322923 | frameshift variant | -/G | delins | 1 |