| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 3 | ||
| rs267606705 | 0.925 | 0.040 | 11 | 119278214 | missense variant | A/G | snv | 1 | |||
| rs121913616 | 0.790 | 0.120 | 1 | 43349337 | missense variant | TG/AA | mnv | 1 | |||
| rs767475870 | 1.000 | 0.040 | 4 | 105276203 | missense variant | C/T | snv | 1 | |||
| rs121912657 | 0.683 | 0.480 | 17 | 7673806 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 |