| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs9838771 | 3 | 30657290 | intron variant | G/A | snv | 2.5E-02 | 3 | ||||
| rs10212320 | 3 | 30632373 | non coding transcript exon variant | C/T | snv | 7.2E-03 | 2 | ||||
| rs12493607 | 0.882 | 0.080 | 3 | 30641447 | intron variant | G/C;T | snv | 1 | |||
| rs3773643 | 3 | 30668751 | intron variant | A/G | snv | 0.19 | 1 |