Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121434613 | 0.882 | 0.240 | X | 111194402 | missense variant | C/A | snv | 4 | |||
rs121434614 | 0.925 | 0.200 | X | 111196570 | missense variant | G/C | snv | 3 | |||
rs121434612 | 1.000 | 0.080 | X | 111142119 | missense variant | C/T | snv | 2 | |||
rs121434611 | 1.000 | 0.080 | X | 111196488 | stop gained | C/T | snv | 1 | |||
rs1569398769 | 1.000 | 0.080 | X | 111142200 | splice region variant | A/G | snv | 1 | |||
rs780775497 | 1.000 | 0.080 | X | 111147758 | stop gained | C/A;T | snv | 1 |