| 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 | ||
| 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 | ||
| rs41315493 | 0.851 | 0.120 | 3 | 38550521 | missense variant | C/A;T | snv | 6.6E-03; 9.7E-05 | 4 | ||
| rs765669597 | 0.851 | 0.120 | 3 | 38614063 | stop gained | A/C;T | snv | 4.7E-06 | 4 | ||
| rs137854617 | 0.882 | 0.120 | 3 | 38581002 | stop gained | C/A;T | snv | 1.1E-04 | 1.5E-04 | 3 | |
| rs36210423 | 0.882 | 0.120 | 3 | 38603887 | missense variant | G/A;C;T | snv | 2.1E-04; 4.9E-03 | 3 | ||
| rs199473112 | 0.925 | 0.080 | 3 | 38605956 | missense variant | G/A;C | snv | 4.1E-06; 5.3E-05 | 2 | ||
| rs199473060 | 1.000 | 3 | 38622468 | missense variant | C/T | snv | 4.1E-06 | 7.0E-06 | 1 | ||
| rs199473111 | 1.000 | 3 | 38606007 | stop gained | C/A;T | snv | 4.8E-05 | 6.3E-05 | 1 | ||
| rs199473115 | 1.000 | 3 | 38604837 | missense variant | G/A;C | snv | 1.2E-05; 8.0E-06 | 1 | |||
| rs199473197 | 1.000 | 3 | 38576780 | missense variant | G/A;C;T | snv | 2.5E-05 | 1 | |||
| rs199473335 | 1.000 | 3 | 38550411 | missense variant | G/T | snv | 8.8E-06 | 3.5E-05 | 1 | ||
| rs199473579 | 1.000 | 3 | 38598978 | stop gained | C/A;T | snv | 4.0E-06 | 7.0E-06 | 1 | ||
| rs199473635 | 1.000 | 3 | 38550896 | missense variant | G/A | snv | 1.6E-05 | 1.4E-05 | 1 |