| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1559931177 | 0.827 | 0.120 | 3 | 49047207 | stop gained | G/A | snv | 34 | |||
| rs781565158 | 0.851 | 0.120 | 12 | 21452130 | missense variant | A/G | snv | 4.7E-05 | 2.1E-05 | 22 | |
| rs1057518083 | 0.851 | 0.120 | 14 | 101986552 | missense variant | C/T | snv | 21 | |||
| rs201518227 | 1.000 | 1 | 179917914 | missense variant | C/T | snv | 3.2E-05 | 5.6E-05 | 13 | ||
| rs757082154 | 1.000 | 0.120 | 2 | 178527491 | stop gained | G/A | snv | 1.2E-05 | 9 | ||
| rs760768093 | 0.882 | 0.160 | 2 | 178533255 | frameshift variant | C/- | delins | 2.4E-05 | 1.4E-05 | 7 | |
| rs150168522 | 0.925 | 0.160 | 21 | 46132367 | missense variant | G/A;C | snv | 4.9E-05; 2.9E-05 | 4 | ||
| rs144133542 | 2 | 55181606 | missense variant | C/A;T | snv | 2.7E-04 | 1 |