| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 101 | ||
| rs121434592 | 0.595 | 0.640 | 14 | 104780214 | missense variant | C/T | snv | 4.0E-06 | 54 | ||
| rs121913275 | 0.672 | 0.320 | 3 | 179218305 | missense variant | G/A;C;T | snv | 4.0E-06 | 26 | ||
| rs121913286 | 0.677 | 0.280 | 3 | 179218306 | missense variant | C/A;G | snv | 23 | |||
| rs121913283 | 0.724 | 0.440 | 3 | 179234286 | missense variant | G/A;T | snv | 4.0E-06 | 16 | ||
| rs121913272 | 0.752 | 0.400 | 3 | 179210192 | missense variant | T/C;G | snv | 13 | |||
| rs397514565 | 0.882 | 0.240 | 3 | 179204576 | missense variant | G/A | snv | 3 | |||
| rs1560137609 | 0.925 | 0.080 | 3 | 179199743 | frameshift variant | -/T | delins | 2 | |||
| rs863225060 | 0.925 | 0.120 | 3 | 179199136 | missense variant | C/T | snv | 2 |