| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10888095 | 0.925 | 0.040 | 8 | 15004905 | intron variant | C/A;G | snv | 2 | |||
| rs10216809 | 0.925 | 0.080 | 8 | 14507414 | intron variant | C/G;T | snv | 1 | |||
| rs11203649 | 8 | 14659785 | intron variant | T/C | snv | 0.72 | 1 | ||||
| rs10097849 | 8 | 14672342 | intron variant | T/G | snv | 0.55 | 1 |