| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 28 | ||
| rs121908029 | 0.763 | 0.200 | 19 | 11105588 | stop gained | G/A;C;T | snv | 1.6E-05; 1.6E-05; 8.1E-06 | 13 | ||
| rs879254850 | 0.776 | 0.160 | 19 | 11113365 | missense variant | A/G;T | snv | 4.0E-06 | 9 | ||
| rs374603772 | 0.776 | 0.160 | 1 | 55058630 | missense variant | C/T | snv | 4.4E-05 | 2.8E-05 | 9 | |
| rs28362261 | 0.851 | 0.160 | 1 | 55058129 | missense variant | A/G | snv | 1.2E-03 | 4.8E-03 | 6 | |
| rs774439908 | 0.827 | 0.160 | 19 | 11113348 | stop gained | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 5 | ||
| rs1555804717 | 0.882 | 0.120 | 19 | 11111523 | frameshift variant | A/- | del | 4 | |||
| rs267606663 | 0.925 | 0.080 | 19 | 44909021 | missense variant | G/A;C | snv | 7.3E-06 | 3 | ||
| rs875989914 | 0.882 | 0.080 | 19 | 11110760 | missense variant | G/A;C | snv | 1.6E-05 | 3 | ||
| rs771479424 | 0.882 | 0.120 | 1 | 55052764 | stop gained | A/G;T | snv | 1.2E-05 | 3 |