| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1501299 | 0.597 | 0.720 | 3 | 186853334 | intron variant | G/C;T | snv | 52 | |||
| rs822396 | 0.732 | 0.400 | 3 | 186849088 | intron variant | G/A | snv | 0.81 | 16 | ||
| rs80356814 | 0.732 | 0.320 | 1 | 156138697 | synonymous variant | C/T | snv | 8.0E-06 | 15 | ||
| rs2241767 | 0.763 | 0.440 | 3 | 186853407 | intron variant | A/G | snv | 0.10 | 10 |