Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13042395 | 0.752 | 0.160 | 20 | 773867 | intron variant | C/T | snv | 5.9E-02 | 13 | ||
| rs3746803 | 1.000 | 0.080 | 20 | 763738 | missense variant | G/A;C | snv | 0.10; 1.2E-05 | 2 | ||
| rs3746802 | 1.000 | 0.080 | 20 | 763664 | missense variant | T/C | snv | 0.10 | 9.3E-02 | 1 | |
| rs3746804 | 1.000 | 0.080 | 20 | 763771 | missense variant | G/A | snv | 0.19 | 0.19 | 1 |