| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs373526624 | 1.000 | 0.080 | 2 | 178607095 | missense variant | C/T | snv | 7.0E-04 | 1.6E-04 | 1 | |
| rs539470256 | 1.000 | 0.080 | 2 | 178779033 | missense variant | C/T | snv | 1.3E-04 | 7.7E-05 | 1 | |
| rs199642423 | 1.000 | 0.040 | 2 | 178532705 | missense variant | C/T | snv | 2.8E-05 | 4.9E-05 | 1 | |
| rs199684560 | 1.000 | 0.080 | 2 | 178633512 | missense variant | G/A | snv | 7.3E-05 | 4.2E-05 | 1 | |
| rs375422359 | 1.000 | 0.040 | 2 | 178563634 | missense variant | C/T | snv | 2.4E-05 | 3.5E-05 | 1 | |
| rs397517792 | 1.000 | 0.120 | 2 | 178764802 | missense variant | G/A | snv | 8.0E-06 | 2.8E-05 | 1 | |
| rs778634417 | 1.000 | 0.160 | 2 | 178633467 | missense variant | C/T | snv | 1.6E-05 | 2.1E-05 | 1 | |
| rs375029799 | 1.000 | 0.040 | 2 | 178776873 | missense variant | C/T | snv | 2.4E-05 | 2.1E-05 | 1 | |
| rs1336054298 | 1.000 | 0.080 | 2 | 178590298 | missense variant | A/G | snv | 1.4E-05 | 1 | ||
| rs369098292 | 1.000 | 0.040 | 2 | 178572742 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs1204056923 | 1.000 | 0.040 | 2 | 178590160 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
| rs397517769 | 1.000 | 0.080 | 2 | 178542408 | missense variant | C/T | snv | 5.6E-05 | 1.4E-05 | 1 | |
| rs139517732 | 0.851 | 0.040 | 2 | 178802273 | missense variant | C/T | snv | 4.4E-05 | 1.4E-05 | 1 | |
| rs1383995916 | 1.000 | 0.080 | 2 | 178589623 | missense variant | A/T | snv | 7.0E-06 | 1 | ||
| rs370004591 | 1.000 | 0.080 | 2 | 178776789 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs756924372 | 1.000 | 0.080 | 2 | 178534461 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs1003158162 | 1.000 | 0.080 | 2 | 178531968 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs55713867 | 1.000 | 0.080 | 2 | 178575658 | missense variant | A/G | snv | 1 | |||
| rs564777385 | 1.000 | 0.040 | 2 | 178800635 | missense variant | C/G;T | snv | 3.6E-05 | 1 | ||
| rs1458591077 | 1.000 | 0.040 | 2 | 178630352 | missense variant | C/T | snv | 1 | |||
| rs764005465 | 1.000 | 0.040 | 2 | 178572808 | missense variant | C/T | snv | 8.1E-06 | 1 | ||
| rs267599092 | 1.000 | 0.040 | 2 | 178779043 | missense variant | C/T | snv | 1 | |||
| rs374713701 | 1.000 | 0.040 | 2 | 178593660 | missense variant | C/A;T | snv | 4.0E-06; 8.1E-06 | 1 | ||
| rs751398376 | 1.000 | 0.080 | 2 | 178609836 | missense variant | C/A;G | snv | 1.2E-05; 4.0E-06 | 1 | ||
| rs149061352 | 1.000 | 0.080 | 2 | 178785717 | missense variant | G/A;T | snv | 4.4E-05; 4.0E-06 | 1 |