| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1556022962 | X | 133304782 | missense variant | C/T | snv | 1 | |||||
| rs1555610590 | 17 | 822445 | stop gained | G/A | snv | 1 | |||||
| rs1379395211 | 17 | 82032779 | missense variant | C/G;T | snv | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1556022962 | X | 133304782 | missense variant | C/T | snv | 1 | |||||
| rs1555610590 | 17 | 822445 | stop gained | G/A | snv | 1 | |||||
| rs1379395211 | 17 | 82032779 | missense variant | C/G;T | snv | 1 |