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 | |||
rs267606891 | 0.882 | 0.200 | MT | 10197 | missense variant | G/A | snv | 2 | |||
rs199476135 | 0.882 | 0.120 | MT | 9176 | missense variant | T/C;G | snv | 2 | |||
rs267606892 | 1.000 | 0.080 | MT | 10563 | missense variant | T/C | snv | 1 | |||
rs199476138 | 0.882 | 0.120 | MT | 9185 | missense variant | T/C | snv | 1 | |||
rs200613617 | 1.000 | 0.160 | MT | 9804 | missense variant | G/A | snv | 1 | |||
rs193302933 | 1.000 | 0.160 | MT | 10664 | synonymous variant | C/T | snv | 1 | |||
rs199476134 | 1.000 | 0.160 | MT | 9101 | missense variant | T/C | snv | 1 | |||
rs267606611 | 1.000 | 0.160 | MT | 9438 | missense variant | G/A | snv | 1 | |||
rs387906422 | 0.925 | 0.040 | MT | 8528 | start lost | T/C | snv | 1 | |||
rs794726857 | 0.925 | 0.200 | MT | 8969 | missense variant | G/A | snv | 1 | |||
rs267606890 | 0.925 | 0.120 | MT | 10191 | missense variant | T/C | snv | 1 | |||
rs199476117 | 0.925 | 0.120 | MT | 10158 | missense variant | T/C | snv | 1 |