| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11118838 | 1.000 | 0.080 | 1 | 221724004 | intron variant | A/C;T | snv | 1 | |||
| rs12724393 | 1.000 | 0.080 | 1 | 221723183 | intron variant | C/A;G | snv | 1 | |||
| rs908858 | 1.000 | 0.080 | 1 | 221709883 | intron variant | C/T | snv | 0.58 | 1 |