| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13002158 | 2 | 143264143 | intron variant | A/G | snv | 0.22 | 1 | ||||
| rs62171698 | 2 | 143201527 | intron variant | C/A;T | snv | 1 | |||||
| rs78490412 | 1.000 | 0.040 | 2 | 143405256 | intron variant | C/T | snv | 0.22 | 1 | ||
| rs13010737 | 1.000 | 0.040 | 2 | 143442474 | intron variant | G/A | snv | 0.36 | 1 | ||
| rs6734367 | 2 | 143556678 | intron variant | T/A;G | snv | 1 |