| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894342 | 0.882 | 0.040 | 12 | 4379372 | missense variant | T/C | snv | 1.6E-05 | 1.4E-05 | 3 | |
| rs104894344 | 0.925 | 0.120 | 12 | 4370713 | missense variant | G/A | snv | 2 | |||
| rs104894343 | 1.000 | 12 | 4372622 | missense variant | A/G | snv | 1 | ||||
| rs772964687 | 1.000 | 12 | 4370630 | missense variant | A/G | snv | 8.0E-06 | 1 |