| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4717806 | 0.776 | 0.200 | 7 | 73702147 | intron variant | T/A;C | snv | 9 | |||
| rs3796863 | 0.790 | 0.160 | 4 | 15848363 | intron variant | G/T | snv | 0.41 | 8 | ||
| rs6449197 | 0.882 | 0.120 | 4 | 15813299 | intron variant | C/T | snv | 0.23 | 3 | ||
| rs2293485 | 1.000 | 0.080 | 7 | 73708593 | synonymous variant | A/G | snv | 1 |