| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
| rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
| rs3775292 | 0.851 | 0.080 | 4 | 186081871 | non coding transcript exon variant | C/G | snv | 0.82 | 5 | ||
| rs7668666 | 1.000 | 4 | 186080138 | intron variant | C/A;T | snv | 4 | ||||
| rs723526 | 1.000 | 7 | 55067126 | intron variant | A/G | snv | 0.86 | 2 |