Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1569146993 | 0.851 | 0.320 | 22 | 42211700 | frameshift variant | -/C | delins | 5 | |||
rs1060505041 | 0.716 | 0.400 | 19 | 13136099 | missense variant | C/A;T | snv | 34 | |||
rs878853165 | 0.882 | 0.200 | 19 | 12843558 | missense variant | C/T | snv | 6 | |||
rs1135401778 | 0.752 | 0.400 | 17 | 67854315 | frameshift variant | T/- | del | 20 | |||
rs767961672 | 0.925 | 0.200 | 14 | 28767822 | missense variant | G/A;T | snv | 4.0E-06 | 4 | ||
rs886041095 | 0.827 | 0.160 | 12 | 13571930 | missense variant | C/T | snv | 11 | |||
rs796052676 | 0.807 | 0.200 | 8 | 132180246 | missense variant | G/A | snv | 7 | |||
rs869312698 | 0.925 | 0.160 | 5 | 88804785 | missense variant | C/T | snv | 5 | |||
rs1553920379 | 0.776 | 0.160 | 4 | 101032294 | frameshift variant | -/AGTA | delins | 27 | |||
rs1085307451 | 0.925 | 0.160 | 3 | 47848246 | missense variant | C/T | snv | 4 | |||
rs1553654413 | 0.925 | 0.240 | 3 | 4627877 | splice region variant | CGTA/- | delins | 4 | |||
rs371582179 | 0.827 | 0.280 | 3 | 33014057 | missense variant | T/C | snv | 3.6E-05 | 6.3E-05 | 7 | |
rs72555360 | 0.807 | 0.280 | 3 | 33058221 | missense variant | G/A | snv | 4.4E-05 | 6.3E-05 | 8 | |
rs869312664 | 0.925 | 0.160 | 2 | 165386920 | stop gained | G/A;T | snv | 4 | |||
rs878853163 | 0.925 | 0.200 | 2 | 199323850 | stop gained | T/A;C | snv | 4 | |||
rs869312671 | 0.882 | 0.160 | 1 | 11144735 | missense variant | C/T | snv | 5 |