Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63750215 | 0.701 | 0.240 | 1 | 226885603 | missense variant | A/T | snv | 19 | |||
rs63750522 | 0.827 | 0.120 | 14 | 73173644 | missense variant | G/A;C | snv | 8 | |||
rs6910730 | 0.925 | 0.080 | 6 | 41278895 | intron variant | A/G | snv | 0.21 | 3 |