| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs201893408 | 0.695 | 0.480 | 8 | 93795970 | missense variant | T/A;C | snv | 8.0E-06; 1.5E-04 | 28 | ||
| rs752362727 | 0.716 | 0.480 | 8 | 93786255 | missense variant | C/T | snv | 2.0E-05 | 22 | ||
| rs1057515576 | 0.807 | 0.280 | 3 | 97787991 | frameshift variant | TAT/GAAAA | delins | 9 | |||
| rs1555487316 | 0.882 | 0.240 | 16 | 20348247 | missense variant | A/C | snv | 5 | |||
| rs1556411578 | X | 108595507 | coding sequence variant | AAGGTGACA/- | delins | 4 | |||||
| rs267606954 | 1.000 | 0.080 | 10 | 94032007 | stop gained | C/T | snv | 2.4E-05 | 3 |