| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913482 | 0.630 | 0.680 | 4 | 1801837 | missense variant | C/T | snv | 35 | |||
| rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 30 | ||
| rs121913483 | 0.649 | 0.560 | 4 | 1801841 | missense variant | C/A;G;T | snv | 4.2E-06; 1.3E-05 | 23 | ||
| rs121913105 | 0.653 | 0.600 | 4 | 1806163 | missense variant | A/C;T | snv | 17 | |||
| rs28933068 | 0.645 | 0.560 | 4 | 1805644 | missense variant | C/A;G;T | snv | 1.6E-05 | 17 | ||
| rs28931614 | 0.672 | 0.520 | 4 | 1804392 | missense variant | G/A;C | snv | 15 | |||
| rs121913116 | 0.763 | 0.360 | 4 | 1799395 | missense variant | C/T | snv | 9 | |||
| rs121913479 | 0.763 | 0.280 | 4 | 1804362 | missense variant | G/A;T | snv | 4.0E-06 | 6 | ||
| rs28931615 | 0.732 | 0.240 | 4 | 1804426 | missense variant | C/A;T | snv | 3 | |||
| rs121913114 | 0.925 | 0.120 | 4 | 1801930 | missense variant | A/G;T | snv | 4.0E-06 | 2 | ||
| rs75790268 | 0.925 | 0.120 | 4 | 1804377 | missense variant | G/T | snv | 1 | |||
| rs144478519 | 0.925 | 0.120 | 2 | 113062547 | stop gained | C/A;T | snv | 4.0E-06; 2.9E-03 | 1 |