Source: CLINVAR
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs878853169 | 1.000 | 0.160 | 13 | 35550528 | stop gained | C/T | snv | 4 | |||
| rs869312667 | 1.000 | 0.160 | 13 | 35157262 | missense variant | C/T | snv | 2 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs878853169 | 1.000 | 0.160 | 13 | 35550528 | stop gained | C/T | snv | 4 | |||
| rs869312667 | 1.000 | 0.160 | 13 | 35157262 | missense variant | C/T | snv | 2 |