| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10821936 | 0.742 | 0.200 | 10 | 61963818 | intron variant | C/T | snv | 0.69 | 11 | ||
| rs11978267 | 0.763 | 0.240 | 7 | 50398606 | intron variant | A/G | snv | 0.25 | 9 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10821936 | 0.742 | 0.200 | 10 | 61963818 | intron variant | C/T | snv | 0.69 | 11 | ||
| rs11978267 | 0.763 | 0.240 | 7 | 50398606 | intron variant | A/G | snv | 0.25 | 9 |