| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3839234 | 5 | 149217131 | non coding transcript exon variant | G/- | delins | 0.39 | 1 | ||||
| rs11743174 | 5 | 149145257 | intron variant | C/T | snv | 0.67 | 1 | ||||
| rs4490572 | 5 | 149232759 | intron variant | G/A;T | snv | 1 | |||||
| rs6884531 | 5 | 149186041 | intron variant | A/G | snv | 0.43 | 1 | ||||
| rs1109114 | 5 | 149236383 | intron variant | C/T | snv | 0.31 | 1 |