Source: CURATED
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4141463 | 0.925 | 0.040 | 20 | 14766825 | intron variant | T/C | snv | 0.50 | 1 | ||
| rs6110458 | 1.000 | 0.040 | 20 | 14882326 | intron variant | C/T | snv | 0.25 | 1 | ||
| rs14135 | 1.000 | 0.040 | 20 | 14884510 | non coding transcript exon variant | T/C | snv | 0.26 | 1 | ||
| rs1475531 | 1.000 | 0.040 | 20 | 14886776 | intron variant | G/T | snv | 0.62 | 1 |