| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912515 | 0.925 | 0.120 | 7 | 150974720 | missense variant | G/A;C;T | snv | 2 | |||
| rs137854619 | 0.925 | 0.120 | 3 | 38550917 | missense variant | C/T | snv | 2.7E-04 | 7.7E-05 | 2 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912515 | 0.925 | 0.120 | 7 | 150974720 | missense variant | G/A;C;T | snv | 2 | |||
| rs137854619 | 0.925 | 0.120 | 3 | 38550917 | missense variant | C/T | snv | 2.7E-04 | 7.7E-05 | 2 |