| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs760112920 | 0.925 | 0.120 | 4 | 54731930 | missense variant | G/T | snv | 4.0E-06 | 3.5E-05 | 2 | |
| rs17368584 | 1.000 | 0.120 | 1 | 76930481 | intron variant | T/A;C | snv | 1 | |||
| rs26532 | 1.000 | 0.120 | 5 | 115837981 | non coding transcript exon variant | C/A | snv | 0.83 | 1 |