| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894673 | 0.776 | 0.160 | 19 | 47839335 | missense variant | C/T | snv | 2.1E-05 | 8 | ||
| rs121434631 | 0.807 | 0.080 | 6 | 42179248 | missense variant | C/G;T | snv | 4.0E-06 | 6 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894673 | 0.776 | 0.160 | 19 | 47839335 | missense variant | C/T | snv | 2.1E-05 | 8 | ||
| rs121434631 | 0.807 | 0.080 | 6 | 42179248 | missense variant | C/G;T | snv | 4.0E-06 | 6 |