| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs75885714 | 3 | 16901018 | intron variant | A/C | snv | 4.6E-02 | 7 | ||||
| rs13412535 | 2 | 224010157 | intron variant | G/A | snv | 0.17 | 5 | ||||
| rs1545747 | 15 | 66164979 | intron variant | G/T | snv | 0.97 | 3 | ||||
| rs79992897 | 2 | 223326960 | intergenic variant | G/C | snv | 7.5E-04 | 1 | ||||
| rs77670845 | 7 | 121229508 | intron variant | ATGAA/- | delins | 0.45 | 1 | ||||
| rs7615304 | 3 | 156957914 | intron variant | A/C;G | snv | 1 |