| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4673 | 0.653 | 0.600 | 16 | 88646828 | missense variant | A/G;T | snv | 0.70 | 32 | ||
| rs1049255 | 0.776 | 0.320 | 16 | 88643329 | 3 prime UTR variant | C/T | snv | 0.49 | 0.48 | 9 | |
| rs1049254 | 0.925 | 0.160 | 16 | 88643420 | missense variant | A/C;G | snv | 8.0E-06; 0.65 | 3 | ||
| rs782047455 | 0.925 | 0.160 | X | 37793674 | missense variant | C/T | snv | 5.5E-06 | 3 |