Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387907043 | 0.925 | 0.120 | 20 | 63930873 | missense variant | T/A;G | snv | 4.0E-06 | 3 | ||
rs587776892 | 0.925 | 0.120 | 20 | 63930871 | inframe deletion | CTC/- | delins | 2 |