| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs72474224 | 0.708 | 0.440 | 13 | 20189473 | missense variant | C/A;T | snv | 7.7E-03 | 18 | ||
| rs28931594 | 0.790 | 0.280 | 13 | 20189434 | missense variant | C/A;T | snv | 9 | |||
| rs35887622 | 0.790 | 0.200 | 13 | 20189481 | missense variant | A/C;G | snv | 8.7E-03 | 8 | ||
| rs17215500 | 0.807 | 0.240 | 11 | 2768881 | stop gained | C/G;T | snv | 1.0E-04 | 7 | ||
| rs74315289 | 0.827 | 0.280 | 1 | 54999325 | missense variant | G/A | snv | 1.0E-04 | 1.5E-04 | 5 | |
| rs111033243 | 0.827 | 0.400 | 7 | 107689112 | missense variant | T/C | snv | 6.1E-04 | 8.1E-04 | 5 | |
| rs2274083 | 0.925 | 0.200 | 13 | 20189241 | missense variant | T/C | snv | 1.5E-02 | 5.1E-03 | 3 | |
| rs753756017 | 0.925 | 0.240 | 10 | 71812296 | intron variant | G/A | snv | 1.5E-04 | 5.0E-04 | 2 | |
| rs148388884 | 1.000 | 0.200 | 1 | 34784871 | missense variant | G/A;C;T | snv | 9.1E-04; 4.4E-05; 8.0E-06 | 1 | ||
| rs760352870 | 1.000 | 0.200 | 7 | 107701196 | splice region variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs759552778 | 1.000 | 0.200 | X | 21743827 | missense variant | T/C | snv | 1.8E-04 | 5.7E-05 | 1 |