| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs869025337 | 0.925 | 0.120 | 6 | 105124593 | missense variant | G/A;C | snv | 4.0E-06 | 5 | ||
| rs199472936 | 0.882 | 0.120 | 7 | 150951592 | missense variant | C/A;T | snv | 5 | |||
| rs72544141 | 0.925 | 0.120 | 4 | 113348277 | missense variant | A/G | snv | 5.5E-04 | 8.3E-04 | 4 | |
| rs1800172 | 0.925 | 0.120 | 11 | 2847899 | missense variant | G/A;T | snv | 6.2E-03 | 4 | ||
| rs199473024 | 7 | 150947362 | missense variant | T/C | snv | 7.0E-06 | 2 |