Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs281874674 | 0.827 | 0.280 | X | 108597479 | missense variant | G/C;T | snv | 8 | |||
rs104886303 | 0.851 | 0.200 | X | 108695409 | missense variant | T/G | snv | 4 | |||
rs1569492161 | 0.882 | 0.280 | X | 108586729 | missense variant | G/C | snv | 4 | |||
rs104886088 | 0.882 | 0.160 | X | 108582920 | stop gained | G/A;T | snv | 3 | |||
rs104886116 | 0.882 | 0.160 | X | 108591635 | missense variant | G/A | snv | 3 | |||
rs104886302 | 0.925 | 0.160 | X | 108695376 | missense variant | G/A;C | snv | 3 | |||
rs281874657 | 0.925 | 0.160 | X | 108586717 | stop gained | C/T | snv | 3 | |||
rs104886055 | 0.925 | 0.160 | X | 108573628 | missense variant | G/C | snv | 2 | |||
rs104886056 | 0.925 | 0.160 | X | 108573637 | missense variant | G/C;T | snv | 2 | |||
rs104886060 | 0.925 | 0.160 | X | 108575937 | missense variant | G/A;T | snv | 2 | |||
rs104886061 | 0.925 | 0.160 | X | 108575947 | missense variant | G/A;T | snv | 2 | |||
rs104886063 | 0.925 | 0.160 | X | 108577953 | missense variant | G/A;T | snv | 2 | |||
rs104886066 | 0.925 | 0.160 | X | 108577980 | missense variant | G/A;T | snv | 2 | |||
rs104886067 | 0.925 | 0.160 | X | 108578078 | missense variant | G/A | snv | 2 | |||
rs104886068 | 0.925 | 0.160 | X | 108578319 | missense variant | G/A | snv | 2 | |||
rs104886074 | 0.925 | 0.160 | X | 108578079 | missense variant | G/A;T | snv | 2 | |||
rs104886075 | 0.925 | 0.160 | X | 108578087 | missense variant | G/A | snv | 2 | |||
rs104886076 | 0.925 | 0.160 | X | 108578291 | missense variant | G/C | snv | 2 | |||
rs104886078 | 0.925 | 0.160 | X | 108580722 | missense variant | G/T | snv | 2 | |||
rs104886080 | 0.925 | 0.160 | X | 108580983 | missense variant | G/A | snv | 2 | |||
rs104886085 | 0.925 | 0.160 | X | 108582902 | missense variant | G/C | snv | 2 | |||
rs104886091 | 0.925 | 0.160 | X | 108582921 | missense variant | G/A | snv | 2 | |||
rs104886092 | 0.925 | 0.160 | X | 108584485 | missense variant | G/T | snv | 2 | |||
rs104886096 | 0.925 | 0.160 | X | 108586676 | missense variant | G/A | snv | 2 | |||
rs104886097 | 0.925 | 0.160 | X | 108586694 | missense variant | G/A | snv | 2 |