| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7578982 | 2 | 111078961 | intron variant | T/C | snv | 0.27 | 2 | ||||
| rs7776054 | 6 | 135097778 | intron variant | A/G | snv | 0.24 | 2 | ||||
| rs913678 | 0.882 | 0.240 | 20 | 50338887 | regulatory region variant | T/C | snv | 0.51 | 1 | ||
| rs9880192 | 1.000 | 0.040 | 3 | 128578726 | upstream gene variant | G/A;C | snv | 0.31 | 1 |