| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267606754 | 0.882 | 0.160 | 17 | 3655307 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 3 | |
| rs121908129 | 0.925 | 0.080 | 17 | 3655101 | missense variant | G/T | snv | 2 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267606754 | 0.882 | 0.160 | 17 | 3655307 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 3 | |
| rs121908129 | 0.925 | 0.080 | 17 | 3655101 | missense variant | G/T | snv | 2 |