| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267607165 | 0.708 | 0.520 | 16 | 89935679 | missense variant | G/A;C | snv | 18 | |||
| rs78861628 | 0.851 | 0.160 | 20 | 5302393 | missense variant | G/A | snv | 3.9E-03 | 1.4E-02 | 4 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267607165 | 0.708 | 0.520 | 16 | 89935679 | missense variant | G/A;C | snv | 18 | |||
| rs78861628 | 0.851 | 0.160 | 20 | 5302393 | missense variant | G/A | snv | 3.9E-03 | 1.4E-02 | 4 |