| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs779530981 | 1.000 | 0.160 | 10 | 87933035 | missense variant | C/A | snv | 4 | |||
| rs1040124120 | 1.000 | 0.160 | 8 | 122953350 | missense variant | C/G;T | snv | 1.6E-05 | 2 | ||
| rs1114167651 | 1.000 | 0.160 | 10 | 87933107 | missense variant | C/A;T | snv | 4.0E-06 | 2 | ||
| rs1239105602 | 1.000 | 0.160 | 10 | 87864168 | 5 prime UTR variant | C/T | snv | 2 | |||
| rs202247812 | 1.000 | 0.160 | 12 | 25225717 | missense variant | T/C | snv | 2 | |||
| rs397507477 | 1.000 | 0.160 | 7 | 140777995 | missense variant | G/A | snv | 2 | |||
| rs917927904 | 1.000 | 0.160 | 10 | 87864242 | 5 prime UTR variant | G/T | snv | 7.0E-06 | 2 | ||
| rs1372399305 | 1.000 | 0.160 | 15 | 88847281 | missense variant | T/A;C | snv | 1 | |||
| rs1375027098 | 1.000 | 0.160 | 3 | 138372947 | frameshift variant | G/- | delins | 7.0E-06 | 1 | ||
| rs1398859175 | 1.000 | 0.160 | 12 | 112477882 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs140074469 | 1.000 | 0.160 | 22 | 39966148 | missense variant | G/A | snv | 7.2E-05 | 3.4E-04 | 1 | |
| rs1553353452 | 1.000 | 0.160 | 2 | 39007033 | missense variant | C/T | snv | 1 | |||
| rs368625677 | 1.000 | 0.160 | 19 | 49637121 | missense variant | C/G;T | snv | 4.1E-06; 3.3E-05 | 1 | ||
| rs3730271 | 1.000 | 0.160 | 3 | 12604195 | missense variant | A/C;G;T | snv | 1 | |||
| rs397507503 | 1.000 | 0.160 | 12 | 112450335 | missense variant | C/T | snv | 1 | |||
| rs397507507 | 1.000 | 0.160 | 12 | 112450358 | missense variant | G/A;C;T | snv | 1 | |||
| rs397507527 | 1.000 | 0.160 | 12 | 112472989 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs397507530 | 1.000 | 0.160 | 12 | 112473033 | missense variant | C/G | snv | 1 | |||
| rs397507544 | 1.000 | 0.160 | 12 | 112489081 | missense variant | C/T | snv | 1 | |||
| rs397509343 | 1.000 | 0.160 | 7 | 140801531 | missense variant | A/C | snv | 1 | |||
| rs397516802 | 1.000 | 0.160 | 12 | 112450397 | missense variant | AC/CT | mnv | 1 | |||
| rs397516803 | 1.000 | 0.160 | 12 | 112450415 | missense variant | C/A | snv | 1 | |||
| rs397516809 | 1.000 | 0.160 | 12 | 112472961 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs397516822 | 1.000 | 0.160 | 3 | 12608823 | missense variant | T/C | snv | 1 | |||
| rs397516825 | 1.000 | 0.160 | 3 | 12604204 | missense variant | T/C | snv | 1 |