Source: BEFREE
| 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 | 62 | ||
| rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 43 | ||
| rs121913273 | 0.605 | 0.440 | 3 | 179218294 | missense variant | G/A;C | snv | 22 | |||
| rs2699887 | 0.763 | 0.280 | 3 | 179148620 | intron variant | C/T | snv | 0.18 | 11 | ||
| rs121913274 | 0.645 | 0.320 | 3 | 179218304 | missense variant | A/C;G;T | snv | 4 | |||
| rs6443626 | 0.851 | 0.200 | 3 | 179237995 | 3 prime UTR variant | T/C | snv | 0.24 | 4 | ||
| rs3976507 | 0.882 | 0.120 | 3 | 179239995 | 3 prime UTR variant | C/T | snv | 0.19 | 0.24 | 3 | |
| rs1057519925 | 0.683 | 0.560 | 3 | 179210291 | missense variant | G/A;C | snv | 1 | |||
| rs1057519941 | 0.776 | 0.240 | 3 | 179203761 | missense variant | T/C;G | snv | 1 | |||
| rs121913272 | 0.752 | 0.400 | 3 | 179210192 | missense variant | T/C;G | snv | 1 | |||
| rs121913286 | 0.677 | 0.280 | 3 | 179218306 | missense variant | C/A;G | snv | 1 | |||
| rs397517201 | 0.732 | 0.240 | 3 | 179218307 | missense variant | A/C;G;T | snv | 1 |