| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs9821797 | 1.000 | 0.040 | 3 | 48680820 | intron variant | T/A | snv | 0.20 | 1 | ||
| rs9839776 | 0.851 | 0.160 | 3 | 181593779 | intron variant | C/G;T | snv | 1 | |||
| rs9874207 | 1.000 | 0.040 | 3 | 70970599 | non coding transcript exon variant | T/C | snv | 0.64 | 1 |