Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137852564 | 0.827 | 0.240 | X | 67722976 | missense variant | G/A;T | snv | 5 | |||
rs137852574 | 0.925 | 0.160 | X | 67723688 | missense variant | T/G | snv | 2 | |||
rs137852588 | 0.925 | 0.160 | X | 67643284 | missense variant | C/T | snv | 2 |