| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1805014 | 0.851 | 0.080 | 16 | 27363708 | missense variant | T/C | snv | 7.4E-03 | 1.4E-02 | 4 | |
| rs1508147 | 1.000 | 0.080 | 17 | 78226507 | upstream gene variant | G/A | snv | 0.38 | 1 | ||
| rs2579931 | 1.000 | 0.080 | 6 | 101406757 | intron variant | G/A;C;T | snv | 1 | |||
| rs9851461 | 1.000 | 0.080 | 3 | 112392234 | downstream gene variant | T/C | snv | 4.9E-02 | 1 | ||
| rs1800810 | 1.000 | 0.080 | 4 | 54227864 | intron variant | C/A;G | snv | 1 |