| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs188674761 | 20 | 55624691 | intron variant | T/A;C | snv | 2 | |||||
| rs6069325 | 1.000 | 0.040 | 20 | 55564428 | intron variant | T/G | snv | 0.14 | 1 | ||
| rs2243930 | 20 | 55572404 | intron variant | G/A | snv | 0.20 | 1 | ||||
| rs2247627 | 20 | 55570028 | intron variant | G/A | snv | 0.44 | 1 | ||||
| rs559267 | 20 | 55582439 | intron variant | A/G | snv | 0.33 | 1 | ||||
| rs559390 | 20 | 55582488 | intron variant | A/T | snv | 0.41 | 1 |