| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1801028 | 0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 | 24 | |
| rs2023239 | 0.724 | 0.160 | 6 | 88150763 | intron variant | T/C | snv | 0.21 | 20 | ||
| rs6675281 | 0.827 | 0.080 | 1 | 231818355 | missense variant | C/T | snv | 0.11 | 0.14 | 7 | |
| rs10042486 | 0.882 | 0.040 | 5 | 63965502 | intron variant | C/T | snv | 0.58 | 4 | ||
| rs7139958 | 1.000 | 0.040 | 13 | 105484383 | intron variant | T/A | snv | 0.32 | 2 |