| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2069762 | 0.672 | 0.560 | 4 | 122456825 | upstream gene variant | A/C | snv | 0.24 | 22 | ||
| rs2069763 | 0.807 | 0.320 | 4 | 122456327 | synonymous variant | C/A | snv | 0.36 | 0.29 | 5 | |
| rs374465594 | 4 | 122451789 | missense variant | A/G | snv | 4.1E-06 | 7.0E-06 | 1 | |||
| rs2069778 | 1.000 | 0.080 | 4 | 122454980 | intron variant | G/A | snv | 0.10 | 1 |