Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63751273 | 0.645 | 0.280 | 17 | 46010389 | missense variant | C/T | snv | 42 | |||
rs63749855 | 0.790 | 0.200 | 17 | 46014271 | missense variant | T/G | snv | 8 | |||
rs533813519 | 0.851 | 0.120 | 1 | 226888097 | missense variant | C/A | snv | 1.9E-04 | 4.2E-05 | 5 | |
rs762046989 | 0.851 | 0.200 | 17 | 45971867 | missense variant | C/G | snv | 8.0E-06 | 5 |