| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs758865890 | 4 | 186288592 | missense variant | T/C | snv | 4.0E-06 | 1 | ||||
| rs780463965 | 19 | 19626638 | missense variant | C/A;T | snv | 4.0E-06; 1.6E-05 | 1 | ||||
| rs759304648 | 0.790 | 0.240 | 9 | 121312479 | synonymous variant | G/A | snv | 8.0E-05 | 3.5E-05 | 9 | |
| rs886043118 | 0.925 | 0.040 | 2 | 191009916 | frameshift variant | T/- | delins | 5 | |||
| rs483352822 | 0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv | 16 | |||
| rs8099917 | 0.581 | 0.600 | 19 | 39252525 | upstream gene variant | T/G | snv | 0.16 | 60 |