Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs132630277 | 1.000 | 0.120 | X | 154420037 | missense variant | G/A | snv | 1 | |||
rs387907218 | 1.000 | 0.120 | X | 154420676 | missense variant | G/A;C | snv | 1 | |||
rs104894937 | 1.000 | 0.120 | X | 154413549 | missense variant | T/C | snv | 1 | |||
rs104894942 | 1.000 | 0.120 | X | 154413248 | missense variant | C/A;T | snv | 1 |