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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
41 | 0.627 | 0.560 | 10 | 87933147 | stop gained | C/G;T | snv | 1.2E-05 | 0.700 | 0 | |||||||
|
6 | 0.827 | 0.240 | 11 | 6617154 | splice acceptor variant | C/A;G;T | snv | 4.0E-04; 1.2E-05 | 0.700 | 0 | |||||||
|
4 | 0.882 | 0.160 | 2 | 166013812 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
7 | 0.827 | 0.160 | 6 | 43007265 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
10 | 0.827 | 0.160 | 9 | 128203609 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
7 | 0.851 | 0.240 | 1 | 42929977 | frameshift variant | AT/- | del | 0.700 | 0 | ||||||||
|
6 | 0.851 | 0.200 | 5 | 83105046 | missense variant | T/C | snv | 1.6E-05 | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||
|
3 | 0.882 | 0.120 | 2 | 1917238 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
|
2 | 1.000 | 0.080 | 3 | 70977021 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 0.010 | 1.000 | 1 | 2019 | 2019 | |||
|
2 | 1.000 | 0.080 | 3 | 70959372 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
|
13 | 0.776 | 0.400 | 1 | 19220814 | frameshift variant | AAGG/- | delins | 1.4E-05 | 0.700 | 1.000 | 2 | 2016 | 2017 |