| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28936670 | 0.708 | 0.280 | 5 | 173235011 | missense variant | G/A | snv | 3.4E-03 | 1.1E-02 | 17 | |
| rs2277923 | 0.752 | 0.160 | 5 | 173235021 | synonymous variant | T/C | snv | 0.41 | 0.44 | 13 | |
| rs104893656 | 0.851 | 0.120 | 2 | 113246826 | missense variant | T/G | snv | 4 | |||
| rs765367813 | 0.882 | 0.120 | 14 | 81143640 | missense variant | C/A;T | snv | 4.0E-06 | 3 | ||
| rs142122217 | 0.925 | 0.080 | 14 | 81142973 | missense variant | T/A;C | snv | 2.4E-04; 4.0E-06 | 2 | ||
| rs55638457 | 1.000 | 0.080 | 7 | 107701183 | missense variant | T/C | snv | 8.3E-03 | 6.0E-03 | 1 |