| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137854618 | 0.742 | 0.120 | 3 | 38566426 | missense variant | C/A;T | snv | 8.0E-06 | 15 | ||
| rs45546039 | 0.732 | 0.120 | 3 | 38613781 | missense variant | C/A;T | snv | 4.1E-06 | 15 | ||
| rs41261344 | 0.763 | 0.120 | 3 | 38575385 | missense variant | C/T | snv | 5.4E-03 | 2.2E-03 | 11 | |
| rs137854601 | 0.776 | 0.120 | 3 | 38551022 | stop gained | C/A;T | snv | 4.0E-06 | 10 | ||
| rs199473097 | 0.763 | 0.120 | 3 | 38606710 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 9 | |
| rs757532106 | 0.763 | 0.120 | 3 | 38550500 | stop gained | G/A | snv | 4.5E-05 | 4.9E-05 | 9 | |
| rs199473119 | 0.790 | 0.120 | 3 | 38604035 | missense variant | G/A;T | snv | 8.4E-06; 4.2E-06 | 7 | ||
| rs137854600 | 0.807 | 0.120 | 3 | 38551504 | missense variant | C/A;T | snv | 6 | |||
| rs199473225 | 0.851 | 0.120 | 3 | 38560397 | missense variant | G/A;C | snv | 6 | |||
| rs12720452 | 0.882 | 0.120 | 3 | 38603758 | missense variant | C/T | snv | 2.9E-04 | 2.9E-04 | 5 | |
| rs199473072 | 0.827 | 0.160 | 3 | 38613773 | missense variant | G/A | snv | 1.2E-05 | 8.4E-05 | 5 | |
| rs199473282 | 0.827 | 0.120 | 3 | 38551513 | missense variant | G/A;T | snv | 4.0E-06 | 5 | ||
| rs41310765 | 0.882 | 0.120 | 3 | 38575424 | missense variant | G/A | snv | 1.4E-04 | 7.7E-05 | 5 | |
| rs137854615 | 0.851 | 0.120 | 3 | 38550989 | missense variant | A/G | snv | 4 | |||
| rs185638763 | 0.882 | 0.120 | 3 | 38599001 | missense variant | G/A;T | snv | 1.2E-05 | 4 | ||
| rs199473604 | 0.882 | 0.120 | 3 | 38560394 | missense variant | G/T | snv | 4 | |||
| rs41315493 | 0.851 | 0.120 | 3 | 38550521 | missense variant | C/A;T | snv | 6.6E-03; 9.7E-05 | 4 | ||
| rs72549410 | 0.851 | 0.120 | 3 | 38606058 | missense variant | C/T | snv | 4 | |||
| rs765669597 | 0.851 | 0.120 | 3 | 38614063 | stop gained | A/C;T | snv | 4.7E-06 | 4 | ||
| rs79299226 | 0.851 | 0.120 | 3 | 38550898 | missense variant | A/G | snv | 4 | |||
| rs137854609 | 0.882 | 0.120 | 3 | 38581170 | missense variant | C/A;T | snv | 7.9E-05 | 3 | ||
| rs137854613 | 0.882 | 0.120 | 3 | 38551505 | stop gained | G/A;T | snv | 3 | |||
| rs137854614 | 0.882 | 0.120 | 3 | 38550988 | missense variant | T/C | snv | 3 | |||
| rs137854617 | 0.882 | 0.120 | 3 | 38581002 | stop gained | C/A;T | snv | 1.1E-04 | 1.5E-04 | 3 | |
| rs199473055 | 0.882 | 0.120 | 3 | 38630393 | missense variant | G/A;C | snv | 4.0E-06 | 3 |