| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 144 | ||
| rs180177133 | 0.807 | 0.240 | 16 | 23614089 | frameshift variant | T/- | delins | 1.2E-05 | 1.4E-05 | 9 | |
| rs1764391 | 0.790 | 0.160 | 1 | 34795168 | missense variant | C/G;T | snv | 0.30 | 7 | ||
| rs56302315 | 0.827 | 0.160 | 4 | 55089802 | missense variant | C/T | snv | 5.3E-04 | 4.1E-04 | 5 | |
| rs121913538 | 0.882 | 0.080 | 12 | 25245328 | missense variant | C/A;G | snv | 3 | |||
| rs760881374 | 1.000 | 0.040 | 19 | 35721464 | missense variant | G/A;T | snv | 1.6E-05 | 1 | ||
| rs1206992207 | 1.000 | 0.040 | 12 | 70587201 | frameshift variant | T/- | del | 1 |