| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267605306 | 1.000 | 0.040 | 19 | 14446504 | missense variant | C/G;T | snv | 1.6E-05 | 1 | ||
| rs1484691555 | 1.000 | 0.040 | 20 | 9539512 | missense variant | C/T | snv | 4.0E-06 | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267605306 | 1.000 | 0.040 | 19 | 14446504 | missense variant | C/G;T | snv | 1.6E-05 | 1 | ||
| rs1484691555 | 1.000 | 0.040 | 20 | 9539512 | missense variant | C/T | snv | 4.0E-06 | 1 |