Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs374234147 | 1.000 | 0.040 | 13 | 28057443 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs376588714 | 1.000 | 0.040 | 13 | 28018483 | missense variant | T/C | snv | 2.4E-05 | 1.4E-05 | 1 | |
| rs398122514 | 1.000 | 0.040 | 13 | 28018487 | inframe insertion | -/TCCGGA | delins | 4.0E-06 | 1 | ||
| rs749281035 | 1.000 | 0.040 | 13 | 28018485 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs759272576 | 1.000 | 0.040 | 13 | 28027224 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs772061268 | 1.000 | 0.040 | 13 | 28018487 | missense variant | T/G | snv | 1 | |||
| rs991132188 | 1.000 | 0.040 | 13 | 28018492 | missense variant | T/C | snv | 1 |