Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs202160208 | 0.827 | 0.160 | 3 | 49722056 | missense variant | C/T | snv | 2.9E-04 | 1.8E-04 | 9 | |
| rs142336618 | 0.827 | 0.120 | 3 | 49723648 | missense variant | C/G | snv | 4.5E-06; 7.0E-04 | 5.3E-04 | 5 | |
| rs142908436 | 0.851 | 0.120 | 3 | 49722057 | missense variant | G/A;T | snv | 1.0E-04; 1.2E-05 | 4 | ||
| rs397509425 | 0.882 | 3 | 49722604 | missense variant | G/A | snv | 3.6E-05 | 1.4E-05 | 4 | ||
| rs397509422 | 0.851 | 0.080 | 3 | 49721835 | missense variant | C/G;T | snv | 4.0E-06; 7.6E-05 | 4 | ||
| rs145564018 | 0.882 | 3 | 49722971 | splice donor variant | C/T | snv | 1.4E-05 | 3 | |||
| rs1553691918 | 0.882 | 3 | 49722698 | frameshift variant | GT/- | delins | 3 | ||||
| rs1553691975 | 0.882 | 3 | 49723007 | frameshift variant | -/CT | delins | 3 | ||||
| rs761714818 | 0.882 | 3 | 49722343 | missense variant | A/G | snv | 6.4E-05 | 4.2E-05 | 3 | ||
| rs763971677 | 0.882 | 3 | 49722126 | stop gained | G/A | snv | 4.0E-06 | 3 | |||
| rs771861177 | 0.882 | 3 | 49721765 | missense variant | C/T | snv | 3.7E-05 | 1.4E-05 | 3 | ||
| rs199922550 | 0.882 | 3 | 49721847 | missense variant | C/T | snv | 6.0E-05 | 4.9E-05 | 3 | ||
| rs397509423 | 1.000 | 3 | 49723293 | stop gained | G/A | snv | 1 |