| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912424 | 1.000 | 17 | 63930095 | missense variant | C/T | snv | 1 | ||||
| rs267606711 | 1.000 | 17 | 63930266 | stop gained | G/A | snv | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912424 | 1.000 | 17 | 63930095 | missense variant | C/T | snv | 1 | ||||
| rs267606711 | 1.000 | 17 | 63930266 | stop gained | G/A | snv | 1 |