| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057515576 | 0.807 | 0.280 | 3 | 97787991 | frameshift variant | TAT/GAAAA | delins | 9 | |||
| rs771054395 | 0.882 | 0.120 | 3 | 97784981 | missense variant | T/C | snv | 3.2E-05 | 2.1E-05 | 3 | |
| rs104893678 | 0.925 | 0.120 | 3 | 97788004 | stop gained | C/T | snv | 8.0E-06 | 2 | ||
| rs104893679 | 1.000 | 0.120 | 3 | 97791797 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 2 | |
| rs1559679965 | 0.925 | 0.120 | 3 | 97780221 | splice donor variant | G/C | snv | 2 | |||
| rs104893680 | 1.000 | 0.120 | 3 | 97768199 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs104893681 | 1.000 | 0.120 | 3 | 97791800 | missense variant | T/C;G | snv | 4.0E-06 | 1 |