Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2229080 | 0.742 | 0.320 | 18 | 52906232 | missense variant | C/A;G | snv | 0.45 | 16 | ||
| rs9944880 | 0.882 | 0.120 | 18 | 53125996 | intron variant | G/A | snv | 5.3E-02 | 3 | ||
| rs387906555 | 1.000 | 0.080 | 18 | 53526629 | missense variant | C/A;G;T | snv | 4.0E-06; 8.0E-06 | 1 |