| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs138659167 | 0.807 | 0.320 | 11 | 71435840 | splice acceptor variant | C/A;G | snv | 5.6E-05; 3.9E-03 | 20 | ||
| rs11555217 | 0.882 | 0.160 | 11 | 71441401 | stop gained | C/G;T | snv | 7.7E-04 | 5 | ||
| rs779896782 | 0.882 | 0.160 | 11 | 71439055 | missense variant | A/C;G | snv | 8.0E-06 | 5 |