| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2626552 | 20 | 33797038 | intron variant | C/T | snv | 0.28 | 2 | ||||
| rs910398 | 20 | 33798464 | intron variant | G/A;T | snv | 2 | |||||
| rs62209625 | 20 | 33810284 | intron variant | A/G | snv | 0.13 | 1 | ||||
| rs751634469 | 1.000 | 0.040 | 20 | 33811532 | missense variant | C/A;T | snv | 4.2E-06; 8.5E-06 | 1 |