| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs59490629 | 1.000 | 0.080 | 6 | 107256268 | intron variant | G/A | snv | 8.5E-02 | 2 | ||
| rs118203955 | 1.000 | 6 | 107210483 | stop gained | G/A;C | snv | 4.0E-06; 8.0E-06 | 1 | |||
| rs118203956 | 1.000 | 6 | 107154674 | missense variant | G/A | snv | 3.2E-05 | 2.1E-05 | 1 | ||
| rs61315837 | 6 | 107221343 | intron variant | A/G | snv | 3.3E-02 | 1 | ||||
| rs7772518 | 6 | 107258176 | intron variant | A/G | snv | 1.6E-02 | 1 | ||||
| rs782439454 | 1.000 | 6 | 107154628 | frameshift variant | CT/- | delins | 1.2E-05 | 7.0E-06 | 1 | ||
| rs9486594 | 1.000 | 0.040 | 6 | 107351323 | intron variant | T/A;C | snv | 1 |