Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397515506 | 1.000 | 0.160 | MT | 14568 | missense variant | C/T | snv | 1 | |||
rs28359178 | 0.882 | 0.280 | MT | 13708 | missense variant | G/A | snv | 1 | |||
rs207459995 | 1.000 | 0.080 | MT | 14985 | missense variant | G/A | snv | 1 | |||
rs200336777 | 1.000 | 0.160 | MT | 15812 | missense variant | G/A | snv | 1 | |||
rs387906425 | 1.000 | 0.160 | MT | 13730 | missense variant | G/A | snv | 1 | |||
rs869025186 | 1.000 | 0.160 | MT | 14498 | missense variant | T/C | snv | 1 | |||
rs199476105 | 0.851 | 0.200 | MT | 14459 | missense variant | G/A | snv | 1 | |||
rs199476107 | 0.925 | 0.200 | MT | 14453 | missense variant | G/A | snv | 1 | |||
rs199476106 | 1.000 | 0.160 | MT | 14495 | missense variant | A/G | snv | 1 | |||
rs207459996 | 1.000 | 0.080 | MT | 15572 | missense variant | T/C | snv | 1 | |||
rs41518645 | 0.925 | 0.200 | MT | 15257 | missense variant | G/A | snv | 1 | |||
rs207460003 | 1.000 | 0.040 | MT | 15498 | missense variant | G/A | snv | 1 | |||
rs199476109 | 0.882 | 0.120 | MT | 14487 | missense variant | T/C | snv | 1 | |||
rs199476104 | 0.925 | 0.160 | MT | 14484 | missense variant | T/C | snv | 1 | |||
rs199476108 | 1.000 | 0.160 | MT | 14482 | missense variant | C/A;G | snv | 1 | |||
rs387906424 | 0.925 | 0.200 | MT | 14596 | missense variant | A/T | snv | 1 |