| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs225014 | 0.695 | 0.400 | 14 | 80203237 | missense variant | T/C | snv | 0.41 | 0.39 | 22 | |
| rs879255589 | 1.000 | 0.040 | 19 | 45478610 | intron variant | G/A;C | snv | 1 | |||
| rs119461976 | 1.000 | 0.040 | 9 | 89348095 | missense variant | G/A | snv | 1.2E-05 | 1 | ||
| rs119461977 | 1.000 | 0.040 | 9 | 89341356 | stop gained | A/G;T | snv | 1.2E-05 | 1 | ||
| rs730880269 | 1.000 | 0.040 | 9 | 89338609 | intron variant | G/A | snv | 1 |