| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 18 | |
| rs4384683 | 18 | 52852662 | intron variant | G/A | snv | 0.56 | 1 | ||||
| rs1453867 | 2 | 232053189 | intron variant | C/T | snv | 0.56 | 1 | ||||
| rs7833174 | 8 | 129706526 | intron variant | T/C;G | snv | 1 | |||||
| rs12310519 | 12 | 23822285 | intron variant | C/T | snv | 0.17 | 1 |