| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137852636 | 1.000 | 0.080 | 1 | 119764211 | missense variant | A/G | snv | 1.0E-04 | 3.5E-05 | 1 | |
| rs137852638 | 1.000 | 0.080 | 1 | 119759915 | missense variant | C/T | snv | 2.2E-04 | 2.6E-04 | 1 | |
| rs137852639 | 1.000 | 0.080 | 1 | 119750830 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs137852640 | 1.000 | 0.080 | 1 | 119764231 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs1553240165 | 1.000 | 0.080 | 1 | 119755599 | splice acceptor variant | T/- | del | 1 | |||
| rs1553240525 | 1.000 | 0.080 | 1 | 119759196 | frameshift variant | A/- | delins | 1 | |||
| rs28937320 | 1.000 | 0.080 | 1 | 119764571 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
| rs764706394 | 1.000 | 0.080 | 1 | 119755426 | splice donor variant | C/G | snv | 1.2E-05 | 1 |