Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs374997012 | 0.851 | 0.280 | 10 | 100989114 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 9 | |
rs80356529 | 0.827 | 0.240 | 3 | 193643996 | missense variant | G/A;C | snv | 9 | |||
rs886037832 | 0.851 | 0.280 | 10 | 100988541 | frameshift variant | T/- | delins | 9 |