Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780533096 | 0.701 | 0.600 | 13 | 23886338 | missense variant | C/G;T | snv | 4.8E-06; 9.6E-06 | 44 | ||
rs1556620697 | 0.827 | 0.360 | X | 124365758 | splice region variant | C/G | snv | 10 | |||
rs1555600214 | 0.925 | 0.040 | 17 | 75830577 | splice donor variant | C/T | snv | 5 | |||
rs1555601863 | 0.925 | 0.040 | 17 | 75836430 | splice acceptor variant | C/T | snv | 5 |