| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1554601483 | 1.000 | 0.120 | 8 | 118110209 | missense variant | T/C | snv | 1 | |||
| rs188859975 | 1.000 | 0.120 | 8 | 117819755 | missense variant | G/A | snv | 2.5E-04 | 7.7E-05 | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1554601483 | 1.000 | 0.120 | 8 | 118110209 | missense variant | T/C | snv | 1 | |||
| rs188859975 | 1.000 | 0.120 | 8 | 117819755 | missense variant | G/A | snv | 2.5E-04 | 7.7E-05 | 1 |