| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 7 | ||
| rs121913273 | 0.605 | 0.440 | 3 | 179218294 | missense variant | G/A;C | snv | 5 | |||
| rs121913105 | 0.653 | 0.600 | 4 | 1806163 | missense variant | A/C;T | snv | 4 | |||
| rs121913479 | 0.763 | 0.280 | 4 | 1804362 | missense variant | G/A;T | snv | 4.0E-06 | 4 | ||
| rs121913482 | 0.630 | 0.680 | 4 | 1801837 | missense variant | C/T | snv | 4 | |||
| rs121913483 | 0.649 | 0.560 | 4 | 1801841 | missense variant | C/A;G;T | snv | 4.2E-06; 1.3E-05 | 4 | ||
| rs78311289 | 0.689 | 0.440 | 4 | 1806162 | missense variant | A/C;G | snv | 4.0E-06 | 4 | ||
| rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 4 | ||
| rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 3 | ||
| rs121913274 | 0.645 | 0.320 | 3 | 179218304 | missense variant | A/C;G;T | snv | 3 | |||
| rs121913484 | 0.851 | 0.240 | 4 | 1804365 | missense variant | A/T | snv | 2 | |||
| rs121913485 | 0.716 | 0.400 | 4 | 1804372 | missense variant | A/G | snv | 2 | |||
| rs104894230 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 2 | |||
| rs121913237 | 0.611 | 0.560 | 1 | 114716126 | missense variant | C/A;G;T | snv | 8.0E-06 | 2 | ||
| rs28931615 | 0.732 | 0.240 | 4 | 1804426 | missense variant | C/A;T | snv | 1 | |||
| rs121913281 | 0.623 | 0.520 | 3 | 179234296 | missense variant | C/T | snv | 1 |