| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs763098832 | 0.882 | 0.120 | 19 | 18783189 | missense variant | G/C;T | snv | 4.1E-06 | 3 | ||
| rs764256352 | 0.882 | 0.120 | 5 | 149981625 | missense variant | G/C | snv | 4.0E-06 | 2.1E-05 | 3 | |
| rs867986409 | 0.882 | 0.120 | 19 | 18784246 | missense variant | C/T | snv | 8.0E-06 | 3 |