Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63750579 | 0.742 | 0.280 | 21 | 25891856 | missense variant | C/G;T | snv | 13 | |||
rs63750311 | 0.790 | 0.240 | 14 | 73192647 | missense variant | A/C | snv | 8 | |||
rs63750671 | 0.790 | 0.240 | 21 | 25891858 | missense variant | G/C | snv | 8 | |||
rs79524815 | 0.851 | 0.240 | 7 | 18658708 | intron variant | T/G | snv | 3.8E-02 | 4 | ||
rs1412095491 | 0.882 | 0.200 | 21 | 26051053 | missense variant | C/G | snv | 4.0E-06 | 3 | ||
rs34487851 | 0.882 | 0.200 | 2 | 106026098 | regulatory region variant | A/G | snv | 0.28 | 3 |