| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs261332 | 0.851 | 0.120 | 15 | 58435126 | non coding transcript exon variant | A/G | snv | 0.80 | 17 | ||
| rs261342 | 15 | 58438954 | intron variant | G/A;C;T | snv | 3 | |||||
| rs261334 | 15 | 58434545 | intron variant | G/C | snv | 0.73 | 3 | ||||
| rs588136 | 15 | 58438299 | intron variant | C/G;T | snv | 2 | |||||
| rs261336 | 15 | 58450219 | intron variant | G/A | snv | 0.81 | 1 | ||||
| rs12914626 | 1.000 | 0.040 | 15 | 58446224 | intron variant | C/T | snv | 0.54 | 1 | ||
| rs7182229 | 15 | 58472984 | intron variant | T/A;C;G | snv | 1 |