| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs779545541 | 0.882 | 0.120 | 14 | 66965293 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
| rs141441277 | 0.882 | 0.120 | X | 100689933 | missense variant | G/A | snv | 5.6E-04 | 3.8E-04 | 5 | |
| rs1800692 | 0.925 | 0.120 | 12 | 6333180 | missense variant | A/G | snv | 0.64 | 0.71 | 5 | |
| rs863225119 | 0.882 | 0.080 | 1 | 201359632 | missense variant | T/A | snv | 5 | |||
| rs367557471 | 1.000 | 0.120 | 8 | 60822055 | stop gained | C/A;T | snv | 5.2E-05 | 7.0E-05 | 4 | |
| rs56208331 | 0.925 | 0.080 | 8 | 11758419 | missense variant | G/A;T | snv | 2.0E-03 | 4 | ||
| rs387906816 | 0.882 | 0.080 | 18 | 22171695 | missense variant | G/A | snv | 8.4E-04 | 1.5E-04 | 4 | |
| rs1340513 | 0.882 | 0.120 | 9 | 6977633 | intron variant | G/A | snv | 0.75 | 4 | ||
| rs398123278 | 0.925 | 0.120 | 6 | 49459376 | stop gained | G/A | snv | 1.6E-05 | 2.8E-05 | 4 | |
| rs199865688 | 0.925 | 0.080 | 11 | 47337496 | missense variant | C/T | snv | 1.5E-03 | 1.2E-03 | 4 | |
| rs1554093433 | 0.925 | 0.080 | 5 | 173232833 | stop gained | G/T | snv | 4 | |||
| rs1557962794 | 0.882 | 0.160 | 1 | 155910693 | missense variant | T/G | snv | 4 | |||
| rs762292772 | 0.882 | 0.160 | 22 | 50721505 | frameshift variant | G/-;GG | delins | 4 | |||
| rs1555226315 | 0.925 | 0.120 | 12 | 114398639 | stop gained | C/T | snv | 4 | |||
| rs769402060 | 0.925 | 0.120 | 2 | 38075022 | missense variant | A/G | snv | 3.3E-05 | 4.2E-05 | 3 | |
| rs886042604 | 1.000 | 0.120 | X | 33020138 | splice donor variant | C/G;T | snv | 3 | |||
| rs2298444 | 0.925 | 0.120 | 11 | 72221370 | intron variant | T/C | snv | 0.27 | 3 | ||
| rs387906772 | 1.000 | 0.080 | 8 | 11755064 | missense variant | A/G;T | snv | 3 | |||
| rs4841587 | 1.000 | 0.080 | 8 | 11756666 | non coding transcript exon variant | G/T | snv | 0.37 | 3 | ||
| rs4841588 | 1.000 | 0.080 | 8 | 11756716 | non coding transcript exon variant | G/T | snv | 0.19 | 3 | ||
| rs1555628863 | 0.925 | 0.080 | 18 | 22172215 | frameshift variant | G/- | delins | 3 | |||
| rs746503158 | 1.000 | 0.040 | 10 | 133420125 | missense variant | A/G;T | snv | 8.0E-06; 4.0E-06 | 3 | ||
| rs104893907 | 1.000 | 5 | 173232776 | stop gained | A/C;T | snv | 3 | ||||
| rs3729753 | 1.000 | 0.040 | 5 | 173232938 | synonymous variant | C/G | snv | 9.9E-03 | 2.2E-03 | 3 | |
| rs2228638 | 1.000 | 0.080 | 10 | 33186354 | missense variant | C/T | snv | 0.12 | 9.4E-02 | 3 |