| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs111426349 | 0.882 | 0.120 | 9 | 99149252 | missense variant | C/A;T | snv | 4.0E-06 | 4 | ||
| rs387906697 | 1.000 | 9 | 99146594 | stop gained | C/T | snv | 2 | ||||
| rs387906696 | 9 | 99128891 | missense variant | A/G | snv | 8.0E-06 | 2.8E-05 | 1 | |||
| rs587776865 | 9 | 99128911 | missense variant | G/C | snv | 1 | |||||
| rs587776866 | 9 | 99142534 | splice acceptor variant | A/C | snv | 1 | |||||
| rs757374917 | 9 | 99129005 | missense variant | C/T | snv | 1 |