Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121918075 | 0.752 | 0.280 | 18 | 31598632 | missense variant | A/G | snv | 15 | |||
rs63750579 | 0.742 | 0.280 | 21 | 25891856 | missense variant | C/G;T | snv | 13 | |||
rs28939068 | 0.790 | 0.200 | 20 | 23635330 | missense variant | A/T | snv | 9 | |||
rs63750671 | 0.790 | 0.240 | 21 | 25891858 | missense variant | G/C | snv | 8 |