| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10838738 | 1.000 | 0.080 | 11 | 47641497 | intron variant | A/G | snv | 0.28 | 3 | ||
| rs4752856 | 1.000 | 0.040 | 11 | 47626490 | intron variant | G/A | snv | 0.28 | 3 | ||
| rs3817334 | 1.000 | 0.080 | 11 | 47629441 | intron variant | C/T | snv | 0.36 | 2 | ||
| rs7118178 | 11 | 47637583 | intron variant | G/A | snv | 0.20 | 2 |