| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909210 | 0.708 | 0.200 | 5 | 136046406 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 15 | ||
| rs121909212 | 0.807 | 0.160 | 5 | 136055770 | missense variant | C/A;G;T | snv | 3.2E-04; 3.2E-05; 3.6E-05 | 6 | ||
| rs267607109 | 0.827 | 0.160 | 5 | 136056754 | missense variant | C/A | snv | 5 | |||
| rs267607110 | 0.851 | 0.160 | 5 | 136056769 | missense variant | C/A | snv | 4 |