Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121909231 | 0.667 | 0.600 | 10 | 87961095 | stop gained | C/A;T | snv | 29 | |||
rs121913293 | 0.732 | 0.360 | 10 | 87952142 | missense variant | C/A;T | snv | 18 | |||
rs863224909 | 0.732 | 0.360 | 10 | 87960952 | stop gained | C/A;G | snv | 14 | |||
rs370795352 | 0.742 | 0.360 | 10 | 87933163 | missense variant | T/A;C | snv | 4.0E-06 | 13 | ||
rs1224040268 | 0.742 | 0.360 | 10 | 87931091 | splice donor variant | T/A;C | snv | 7.0E-06 | 12 | ||
rs147232392 | 0.882 | 0.240 | X | 137566740 | missense variant | G/A;T | snv | 2.6E-03 | 1 | ||
rs398122850 | 1.000 | 0.200 | X | 137566853 | inframe insertion | -/GCCGCC | delins | 1 |