| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137854618 | 0.742 | 0.120 | 3 | 38566426 | missense variant | C/A;T | snv | 8.0E-06 | 15 | ||
| rs60682848 | 0.790 | 0.200 | 1 | 156134838 | stop gained | C/T | snv | 7.0E-06 | 11 | ||
| rs150821281 | 0.827 | 0.080 | 12 | 32878461 | missense variant | G/A | snv | 2.3E-03 | 2.5E-03 | 7 | |
| rs200484060 | 1.000 | 18 | 31536370 | missense variant | T/G | snv | 5.6E-05 | 1.4E-05 | 4 | ||
| rs58327533 | 1.000 | 0.120 | 1 | 156114991 | missense variant | C/G;T | snv | 4 |