| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2296972 | 0.925 | 0.080 | 13 | 46854336 | intron variant | A/C | snv | 0.70 | 4 | ||
| rs1885884 | 13 | 46856141 | non coding transcript exon variant | C/A;G;T | snv | 2 | |||||
| rs7984966 | 13 | 46855311 | intron variant | T/A;C | snv | 1 | |||||
| rs643627 | 1.000 | 0.040 | 13 | 46854476 | intron variant | T/C | snv | 0.27 | 1 |