Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1599988 | 1.000 | 0.160 | MT | 4216 | missense variant | T/C | snv | 1 | |||
rs41460449 | 1.000 | 0.160 | MT | 3394 | missense variant | T/C | snv | 1 | |||
rs199476118 | 0.925 | 0.160 | MT | 3460 | missense variant | G/A | snv | 1 | |||
rs199476120 | 1.000 | MT | 3397 | missense variant | A/G | snv | 1 | ||||
rs201212638 | 1.000 | 0.200 | MT | 3398 | missense variant | T/C | snv | 1 | |||
rs199476119 | 1.000 | 0.160 | MT | 4160 | missense variant | T/C | snv | 1 |