| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057519076 | 0.925 | 0.200 | 19 | 43769805 | missense variant | C/A;T | snv | 3 | |||
| rs749288233 | 0.925 | 0.200 | 16 | 88715708 | missense variant | C/T | snv | 6.4E-06 | 2 | ||
| rs544281438 | 1.000 | 0.200 | 16 | 88716650 | missense variant | G/A | snv | 7.2E-05 | 5.6E-05 | 1 |