| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894312 | 0.851 | 0.080 | 11 | 1841468 | stop gained | C/T | snv | 5 | |||
| rs121913623 | 0.882 | 0.080 | 17 | 10648592 | missense variant | C/T | snv | 7.0E-06 | 3 | ||
| rs104894311 | 1.000 | 0.080 | 11 | 1841523 | missense variant | G/A | snv | 1 | |||
| rs199474800 | 1.000 | 0.080 | 11 | 1841498 | inframe deletion | GAG/- | delins | 1 | |||
| rs1555525264 | 1.000 | 0.080 | 17 | 10632606 | missense variant | C/T | snv | 1 | |||
| rs797046046 | 1.000 | 0.080 | 11 | 1841527 | missense variant | G/T | snv | 1 |