| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
| rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
| rs11655081 | 0.851 | 0.080 | 17 | 68386068 | intron variant | T/C | snv | 0.18 | 7 | ||
| rs374512193 | 0.925 | 0.120 | 8 | 42838177 | missense variant | T/C | snv | 5.2E-05 | 5.6E-05 | 4 | |
| rs750424668 | 1.000 | 0.040 | 9 | 77424057 | frameshift variant | GT/- | delins | 8.0E-06 | 7.0E-06 | 1 | |
| rs762418293 | 1.000 | 0.040 | 8 | 42838290 | missense variant | A/G | snv | 1.6E-05 | 6.3E-05 | 1 |