| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7118900 | 11 | 113396099 | missense variant | G/A | snv | 0.25 | 0.25 | 1 | |||
| rs1875999 | 5 | 76969157 | 3 prime UTR variant | T/C | snv | 0.38 | 1 | ||||
| rs2073837 | 9 | 133657806 | intron variant | G/A | snv | 0.31 | 1 | ||||
| rs1075650 | 9 | 129176634 | 3 prime UTR variant | T/C | snv | 0.25 | 1 | ||||
| rs16918875 | 8 | 53229594 | synonymous variant | G/A | snv | 4.3E-02 | 7.1E-02 | 1 | |||
| rs963549 | 8 | 53229264 | synonymous variant | C/T | snv | 0.17 | 0.24 | 1 |