| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913400 | 0.683 | 0.360 | 3 | 41224610 | missense variant | C/A;G;T | snv | 17 | |||
| rs121913228 | 0.742 | 0.200 | 3 | 41224621 | missense variant | T/C;G | snv | 11 | |||
| rs121434264 | 0.851 | 0.080 | 1 | 193125171 | missense variant | T/C | snv | 1 | |||
| rs386134259 | 1.000 | 0.120 | 11 | 64807577 | stop gained | G/A;C;T | snv | 1 | |||
| rs794728648 | 0.925 | 0.120 | 11 | 64808078 | missense variant | C/A;T | snv | 1 |