| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2236496 | 9 | 4844265 | intron variant | T/C | snv | 0.19 | 3 | ||||
| rs2279434 | 10 | 45459616 | intron variant | C/T | snv | 7.1E-02 | 3 | ||||
| rs4916483 | 3 | 196180782 | intergenic variant | T/C | snv | 0.12 | 3 | ||||
| rs563995 | 19 | 43774629 | intron variant | G/A | snv | 0.24 | 0.34 | 3 | |||
| rs632057 | 6 | 139512875 | intron variant | T/G | snv | 0.57 | 3 | ||||
| rs762516 | X | 154536448 | intron variant | C/T | snv | 4.7E-02 | 3 | ||||
| rs9310736 | 3 | 24309320 | intron variant | A/G | snv | 0.69 | 3 |