Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs199476105 | 0.851 | 0.200 | MT | 14459 | missense variant | G/A | snv | 1 | |||
rs199476109 | 0.882 | 0.120 | MT | 14487 | missense variant | T/C | snv | 1 | |||
rs267606893 | 0.925 | 0.120 | MT | 12706 | missense variant | T/C | 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 |