| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3831732 | 10 | 87895485 | intron variant | -/A;AA | delins | 2 | |||||
| rs59085061 | 10 | 87921701 | intron variant | A/G | snv | 5.2E-02 | 1 | ||||
| rs1234214 | 10 | 87938433 | intron variant | C/A | snv | 0.34 | 1 | ||||
| rs741804 | 10 | 87896399 | intron variant | A/C | snv | 3.6E-02 | 1 | ||||
| rs77413490 | 10 | 87921931 | intron variant | G/A;T | snv | 1 |