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 | |||
rs199476115 | 1.000 | 0.160 | MT | 5244 | missense variant | G/A | snv | 1 | |||
rs28357980 | 1.000 | 0.160 | MT | 4917 | missense variant | A/G | snv | 1 | |||
rs267606895 | 0.882 | 0.240 | MT | 13045 | missense variant | A/C | snv | 1 | |||
rs267606898 | 0.851 | 0.240 | MT | 13042 | missense variant | G/A | snv | 1 | |||
rs28359178 | 0.882 | 0.280 | MT | 13708 | missense variant | G/A | snv | 1 | |||
rs397515506 | 1.000 | 0.160 | MT | 14568 | missense variant | C/T | 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 | |||
rs199476118 | 0.925 | 0.160 | MT | 3460 | missense variant | G/A | snv | 1 | |||
rs41460449 | 1.000 | 0.160 | MT | 3394 | missense variant | T/C | snv | 1 | |||
rs199476119 | 1.000 | 0.160 | MT | 4160 | missense variant | T/C | snv | 1 | |||
rs267606611 | 1.000 | 0.160 | MT | 9438 | missense variant | G/A | 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 | |||
rs199476112 | 0.925 | 0.160 | MT | 11778 | missense variant | G/A | snv | 1 | |||
rs199476134 | 1.000 | 0.160 | MT | 9101 | missense variant | T/C | snv | 1 | |||
rs267606899 | 1.000 | 0.160 | MT | 12848 | missense variant | C/T | snv | 1 | |||
rs199476105 | 0.851 | 0.200 | MT | 14459 | missense variant | G/A | snv | 1 | |||
rs869025186 | 1.000 | 0.160 | MT | 14498 | missense variant | T/C | snv | 1 | |||
rs199476106 | 1.000 | 0.160 | MT | 14495 | missense variant | A/G | snv | 1 | |||
rs41518645 | 0.925 | 0.200 | MT | 15257 | missense variant | G/A | 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 |