| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3755955 | 0.925 | 0.080 | 4 | 1000626 | missense variant | G/A;C | snv | 0.16; 8.0E-06 | 4 | ||
| rs6831280 | 0.925 | 0.080 | 4 | 1002377 | missense variant | G/A;C | snv | 0.17 | 4 | ||
| rs28377268 | 0.925 | 0.080 | 9 | 95462774 | intron variant | G/A;C;T | snv | 2 |