| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs397516955 | 0.790 | 0.120 | 6 | 7562753 | stop gained | G/A | snv | 9 | |||
| rs794728137 | 0.807 | 0.120 | 6 | 7565507 | frameshift variant | -/G | delins | 6 | |||
| rs606231295 | 0.925 | 0.120 | 6 | 7570553 | missense variant | C/T | snv | 2 | |||
| rs1184921987 | 1.000 | 6 | 7571528 | missense variant | A/C;G | snv | 1 | ||||
| rs1554107096 | 1.000 | 6 | 7571534 | missense variant | A/C | snv | 1 | ||||
| rs1554107098 | 1.000 | 6 | 7571546 | missense variant | T/C;G | snv | 1 | ||||
| rs606231293 | 1.000 | 6 | 7571496 | inframe insertion | -/GGAAAATACAGTCTCAGTTCACCGATGCCC | delins | 1 | ||||
| rs606231294 | 1.000 | 6 | 7571471 | missense variant | C/T | snv | 1 |