Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
8 | 0.807 | 0.360 | 13 | 108208829 | stop gained | G/A | snv | 9.9E-05 | 7.0E-05 | 0.700 | 1.000 | 2 | 2001 | 2014 | |||
|
8 | 0.776 | 0.280 | 13 | 32380040 | frameshift variant | C/- | delins | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
6 | 0.851 | 0.200 | 5 | 83105046 | missense variant | T/C | snv | 1.6E-05 | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||
|
3 | 0.925 | 0.160 | 13 | 108209756 | frameshift variant | AG/-;AGAG | delins | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
60 | 0.689 | 0.400 | 6 | 42978878 | stop gained | C/T | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
5 | 0.851 | 0.240 | 3 | 142568059 | splice region variant | T/C | snv | 0.700 | 0 | ||||||||
|
5 | 0.851 | 0.240 | 3 | 142507967 | missense variant | C/A | snv | 0.700 | 0 | ||||||||
|
9 | 0.882 | 0.160 | 15 | 48460299 | missense variant | C/A | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.200 | 3 | 52149850 | stop gained | G/A | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
3 | 0.882 | 0.160 | 10 | 68416703 | frameshift variant | G/- | delins | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.160 | 2 | 46623765 | frameshift variant | T/- | delins | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.160 | 2 | 46619676 | frameshift variant | -/GG | delins | 0.700 | 0 | ||||||||
|
64 | 0.672 | 0.400 | 6 | 42978330 | missense variant | G/A | snv | 3.6E-05 | 2.8E-05 | 0.700 | 0 |