| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2572925 | 1.000 | 0.040 | 8 | 142786489 | missense variant | C/G;T | snv | 0.36 | 1 | ||
| rs2585140 | 1.000 | 0.040 | 8 | 142725478 | intron variant | A/G | snv | 0.51 | 1 | ||
| rs28473387 | 1.000 | 0.040 | 8 | 142626112 | intergenic variant | T/C | snv | 0.63 | 1 | ||
| rs2920297 | 1.000 | 0.040 | 8 | 142681665 | 3 prime UTR variant | A/G | snv | 0.44 | 1 | ||
| rs7046863 | 1.000 | 0.040 | 9 | 133246054 | downstream gene variant | T/C | snv | 0.27 | 1 | ||
| rs7775478 | 1.000 | 0.040 | 6 | 65151300 | intron variant | G/T | snv | 0.26 | 1 | ||
| rs9324593 | 1.000 | 0.040 | 8 | 142605634 | intergenic variant | A/G | snv | 0.18 | 1 | ||
| rs975618 | 1.000 | 0.040 | 6 | 65114686 | intron variant | G/A | snv | 0.27 | 1 |