| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs587778816 | 1.000 | 0.120 | 4 | 1803731 | missense variant | C/A;G | snv | 1 | |||
| rs587778817 | 1.000 | 0.120 | 4 | 1803744 | missense variant | A/G;T | snv | 4.0E-06 | 1 | ||
| rs751213196 | 1.000 | 0.120 | 4 | 1805602 | missense variant | G/A;T | snv | 1.2E-05; 4.0E-06 | 1 | ||
| rs773197447 | 1.000 | 0.080 | 4 | 1807159 | missense variant | G/A;C | snv | 3.2E-05; 2.3E-05 | 1 | ||
| rs77722678 | 1.000 | 0.120 | 4 | 1805643 | missense variant | A/C;G | snv | 4.0E-06 | 1 |