| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs386833976 | 1.000 | 0.120 | 13 | 76996008 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs386833977 | 1.000 | 0.120 | 13 | 76996028 | missense variant | C/T | snv | 1 | |||
| rs386833982 | 1.000 | 0.120 | 13 | 77000663 | frameshift variant | A/- | delins | 1 | |||
| rs730882146 | 1.000 | 0.120 | 13 | 77000680 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs750935331 | 1.000 | 0.120 | 13 | 77000850 | stop gained | C/G;T | snv | 4.1E-06 | 1 | ||
| rs764495616 | 1.000 | 0.120 | 13 | 77000685 | stop gained | G/C;T | snv | 1 | |||
| rs780198002 | 1.000 | 0.120 | 13 | 76992229 | frameshift variant | TC/- | delins | 9.5E-06 | 1 | ||
| rs869312751 | 1.000 | 0.120 | 13 | 76996109 | stop gained | C/T | snv | 1 |