Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 59 | |||
rs1280914556 | 1 | 32014269 | missense variant | A/G | snv | 2.1E-05 | 2 | ||||
rs756915170 | 19 | 49909654 | missense variant | T/C | snv | 4.0E-06 | 2 |