| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13098911 | 0.882 | 0.200 | 3 | 46193709 | intron variant | C/G;T | snv | 5 | |||
| rs4987053 | 1.000 | 0.080 | 3 | 46265209 | synonymous variant | T/C | snv | 9.2E-02; 4.0E-06 | 9.1E-02 | 1 | |
| rs755441932 | 1.000 | 0.080 | 3 | 46265165 | missense variant | A/G | snv | 5.8E-05 | 1.4E-05 | 1 |