| 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 | 5 | |
| rs387906813 | 0.882 | 0.080 | 18 | 22181546 | missense variant | A/C;G | snv | 2 | |||
| rs28939675 | 0.882 | 0.200 | 22 | 19763273 | missense variant | T/A | snv | 2 | |||
| rs121908601 | 0.851 | 0.080 | 8 | 105419192 | missense variant | A/C;G | snv | 4.0E-06; 2.7E-03 | 2 | ||
| rs121434423 | 0.925 | 0.080 | 19 | 18868916 | missense variant | C/T | snv | 7.2E-06 | 1 | ||
| rs267606914 | 0.925 | 0.080 | 8 | 23702906 | missense variant | A/G | snv | 1 | |||
| rs202204708 | 0.882 | 0.080 | 8 | 105788864 | missense variant | A/G | snv | 4.5E-04 | 4.7E-04 | 1 |