| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
| rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
| rs12673132 | 0.925 | 7 | 34663912 | intron variant | G/A | snv | 4.2E-02 | 2 | |||
| rs6972158 | 0.925 | 0.080 | 7 | 34849570 | missense variant | A/G | snv | 0.28 | 0.34 | 2 | |
| rs6947841 | 1.000 | 7 | 34834133 | intron variant | C/T | snv | 0.19 | 1 |