Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs199476133 | 0.742 | 0.320 | MT | 8993 | missense variant | T/C;G | snv | 4 | |||
rs794726857 | 0.925 | 0.200 | MT | 8969 | missense variant | G/A | snv | 1 | |||
rs267606894 | 1.000 | 0.200 | MT | 12770 | missense variant | A/G | snv | 1 | |||
rs267606895 | 0.882 | 0.240 | MT | 13045 | missense variant | A/C | snv | 1 | |||
rs267606896 | 0.882 | 0.200 | MT | 13084 | missense variant | A/T | snv | 1 | |||
rs267606897 | 0.882 | 0.200 | MT | 13513 | missense variant | G/A | snv | 1 | |||
rs267606898 | 0.851 | 0.240 | MT | 13042 | missense variant | G/A | snv | 1 | |||
rs201212638 | 1.000 | 0.200 | MT | 3398 | missense variant | T/C | snv | 1 | |||
rs199476113 | 1.000 | 0.200 | MT | 11084 | missense variant | A/G | snv | 1 | |||
rs199476107 | 0.925 | 0.200 | MT | 14453 | missense variant | G/A | snv | 1 |