| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs587777006 | 0.882 | 0.080 | 19 | 42249565 | stop gained | G/A;C | snv | 4.0E-06 | 3 | ||
| rs886041001 | 1.000 | 19 | 42249934 | missense variant | T/C | snv | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs587777006 | 0.882 | 0.080 | 19 | 42249565 | stop gained | G/A;C | snv | 4.0E-06 | 3 | ||
| rs886041001 | 1.000 | 19 | 42249934 | missense variant | T/C | snv | 1 |