| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1566538321 | 1.000 | 0.120 | 13 | 20222994 | frameshift variant | G/- | delins | 1 | |||
| rs772862268 | 1.000 | 0.120 | 13 | 20223159 | stop gained | G/A | snv | 1.2E-05 | 2.8E-05 | 1 | |
| rs370564476 | 1.000 | 0.120 | 17 | 19024372 | missense variant | T/A | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs765136820 | 1.000 | 0.120 | 3 | 122001823 | missense variant | C/G | snv | 1.1E-04 | 2.8E-05 | 1 | |
| rs1465957812 | 1.000 | 0.120 | 10 | 77084649 | missense variant | G/A | snv | 1 | |||
| rs76737438 | 1.000 | 0.120 | 11 | 2570686 | missense variant | G/C | snv | 1 | |||
| rs144964568 | 1.000 | 0.120 | 1 | 34785465 | stop gained | C/T | snv | 2.0E-05 | 1.4E-05 | 1 | |
| rs778568636 | 1.000 | 0.120 | 18 | 46505856 | missense variant | C/A | snv | 6.4E-06 | 1 | ||
| rs756215789 | 1.000 | 0.120 | 11 | 118263084 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs371465450 | 1.000 | 0.120 | 12 | 80255183 | stop gained | C/T | snv | 4.5E-05 | 7.0E-05 | 1 | |
| rs757774496 | 1.000 | 0.120 | 12 | 80279038 | stop gained | C/A;T | snv | 3.4E-05 | 4.2E-05 | 1 | |
| rs1321703512 | 1.000 | 0.120 | 5 | 102477684 | missense variant | A/G | snv | 1.2E-05 | 1 | ||
| rs750584965 | 1.000 | 0.120 | 3 | 46709171 | missense variant | G/A | snv | 2.0E-05 | 1.4E-05 | 1 | |
| rs5756795 | 1.000 | 0.120 | 22 | 37726115 | missense variant | T/C | snv | 0.39 | 0.35 | 1 | |
| rs56002719 | 1.000 | 0.120 | 4 | 6302122 | missense variant | A/T | snv | 3.8E-03 | 3.5E-03 | 1 | |
| rs71524353 | 1.000 | 0.120 | 4 | 6300948 | stop gained | G/A;T | snv | 1.2E-03 | 1 |