Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs188942711 | 0.763 | 0.200 | 2 | 227253336 | missense variant | G/A;T | snv | 2.8E-05; 4.0E-06 | 9 | ||
rs104886142 | 0.790 | 0.280 | X | 108598793 | missense variant | G/A | snv | 8.7E-05 | 4.7E-05 | 10 | |
rs1131692060 | 1.000 | X | 108601404 | missense variant | G/T | snv | 1 | ||||
rs754313620 | 0.925 | 0.080 | 14 | 104714452 | missense variant | T/C;G | snv | 7.0E-06 | 2 | ||
rs756101090 | 1.000 | 20 | 62330867 | missense variant | G/A | snv | 4.1E-05 | 8.4E-05 | 1 | ||
rs11089788 | 0.851 | 0.120 | 22 | 36355056 | intron variant | C/A | snv | 0.46 | 5 | ||
rs61747728 | 0.701 | 0.240 | 1 | 179557079 | missense variant | C/T | snv | 3.0E-02 | 2.8E-02 | 20 |