| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs975618 | 1.000 | 0.040 | 6 | 65114686 | intron variant | G/A | snv | 0.27 | 1 | ||
| rs2572904 | 1.000 | 0.040 | 8 | 142710775 | intron variant | A/C | snv | 0.49 | 1 | ||
| rs2585140 | 1.000 | 0.040 | 8 | 142725478 | intron variant | A/G | snv | 0.51 | 1 | ||
| rs2572925 | 1.000 | 0.040 | 8 | 142786489 | missense variant | C/G;T | snv | 0.36 | 1 | ||
| rs2164308 | 1.000 | 0.040 | 8 | 142704241 | 3 prime UTR variant | C/T | snv | 0.49 | 1 | ||
| rs2244163 | 1.000 | 0.040 | 8 | 142703082 | 3 prime UTR variant | T/G | snv | 0.42 | 0.43 | 1 | |
| rs1045574 | 1.000 | 0.040 | 8 | 142682540 | 3 prime UTR variant | G/A | snv | 0.46 | 0.44 | 1 | |
| rs2920297 | 1.000 | 0.040 | 8 | 142681665 | 3 prime UTR variant | A/G | snv | 0.44 | 1 |