| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1555661490 | 18 | 21505949 | missense variant | G/T | snv | 1 | |||||
| rs1555665627 | 1.000 | 18 | 21520823 | splice donor variant | G/- | delins | 1 | ||||
| rs1555663997 | 1.000 | 18 | 21515583 | missense variant | G/A | snv | 1 | ||||
| rs1555659101 | 1.000 | 18 | 21496602 | stop gained | C/T | snv | 1 | ||||
| rs1555654020 | 1.000 | 18 | 21473099 | missense variant | C/T | snv | 1 | ||||
| rs1555660209 | 1.000 | 18 | 21500568 | frameshift variant | -/C | delins | 1 | ||||
| rs1555664772 | 1.000 | 18 | 21518140 | missense variant | T/G | snv | 1 | ||||
| rs1555661907 | 1.000 | 18 | 21508117 | splice acceptor variant | G/C | snv | 1 | ||||
| rs1555662061 | 1.000 | 18 | 21508556 | missense variant | T/C | snv | 1 | ||||
| rs1555662027 | 1.000 | 18 | 21508463 | missense variant | A/G | snv | 1 | ||||
| rs1555662052 | 1.000 | 18 | 21508536 | stop gained | C/A | snv | 1 | ||||
| rs1555650110 | 1.000 | 18 | 21451082 | stop gained | G/T | snv | 1 | ||||
| rs1311814599 | 1.000 | 18 | 21440302 | missense variant | G/A | snv | 1.4E-05 | 1 | |||
| rs1555649811 | 1.000 | 18 | 21449696 | frameshift variant | C/- | delins | 1 | ||||
| rs377314861 | 18 | 21440307 | missense variant | C/T | snv | 6.3E-06 | 1 | ||||
| rs1567966432 | 18 | 21383629 | missense variant | T/G | snv | 1 | |||||
| rs1555648043 | 18 | 21440301 | stop gained | C/T | snv | 1 |