| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913528 | 0.851 | 0.160 | 12 | 25227349 | missense variant | C/A;T | snv | 12 | |||
| rs1057519090 | 0.851 | 0.160 | 13 | 110492105 | missense variant | G/A | snv | 7 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913528 | 0.851 | 0.160 | 12 | 25227349 | missense variant | C/A;T | snv | 12 | |||
| rs1057519090 | 0.851 | 0.160 | 13 | 110492105 | missense variant | G/A | snv | 7 |