| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1043679457 | 0.752 | 0.400 | 5 | 60927745 | intron variant | C/A;G;T | snv | 33 | |||
| rs727502818 | 0.790 | 0.160 | 11 | 17772053 | missense variant | G/A | snv | 26 | |||
| rs1553281318 | 0.882 | 0.120 | 1 | 226986536 | frameshift variant | -/A | delins | 7 | |||
| rs1555475794 | 0.925 | 0.120 | 16 | 682729 | 3 prime UTR variant | T/C | snv | 7 | |||
| rs730882209 | 0.925 | 0.080 | 9 | 132326375 | frameshift variant | -/C | delins | 6 |