Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121918683 | 1.000 | 0.160 | 8 | 127738519 | missense variant | A/C | snv | 1 | |||
rs63750264 | 0.716 | 0.360 | 21 | 25891784 | missense variant | C/A;G;T | snv | 1 | |||
rs121918685 | 1.000 | 0.160 | 8 | 127738437 | missense variant | C/G | snv | 1 | |||
rs28933407 | 1.000 | 0.160 | 8 | 127738431 | missense variant | C/T | snv | 1 | |||
rs397518423 | 0.790 | 0.240 | 1 | 9726972 | missense variant | G/A | snv | 1 |