| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs775414124 | 0.925 | 0.280 | 18 | 49332008 | splice acceptor variant | T/C | snv | 1.6E-05 | 1.4E-05 | 2 | |
| rs120074161 | 1.000 | 0.280 | 18 | 49430347 | stop gained | G/A;C | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs120074162 | 1.000 | 0.280 | 18 | 49378592 | stop gained | A/G;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs120074163 | 1.000 | 0.280 | 18 | 49257065 | missense variant | T/A | snv | 8.0E-06 | 1 | ||
| rs1568119124 | 1.000 | 0.280 | 18 | 49258494 | splice acceptor variant | C/T | snv | 1 | |||
| rs1568264929 | 1.000 | 0.280 | 18 | 49331864 | frameshift variant | T/- | delins | 1 | |||
| rs1568319747 | 1.000 | 0.280 | 18 | 49363235 | splice acceptor variant | T/C | snv | 1 | |||
| rs1471488189 | 1.000 | 0.280 | 18 | 49044187 | frameshift variant | T/- | delins | 3.2E-05 | 1 |