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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
13 | 0.776 | 0.240 | 2 | 39022772 | missense variant | C/A;G | snv | 0.700 | 0 | ||||||||
|
5 | 0.882 | 0.160 | 12 | 112446385 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
10 | 0.790 | 0.240 | 12 | 112450408 | missense variant | G/C;T | snv | 0.700 | 0 | ||||||||
|
8 | 0.827 | 0.160 | 12 | 112450497 | missense variant | A/C | snv | 0.700 | 0 | ||||||||
|
20 | 0.708 | 0.560 | 12 | 112489083 | missense variant | G/A;C | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
27 | 0.776 | 0.200 | 2 | 39023128 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
7 | 0.827 | 0.160 | 2 | 39023118 | missense variant | A/C;G | snv | 0.700 | 0 | ||||||||
|
18 | 0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
17 | 0.752 | 0.320 | 12 | 25245277 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.040 | 19 | 42224882 | missense variant | A/C | snv | 0.700 | 0 | ||||||||
|
19 | 0.701 | 0.520 | 1 | 165743172 | stop gained | G/A | snv | 1.2E-05 | 2.1E-05 | 0.700 | 0 | ||||||
|
14 | 0.776 | 0.360 | 16 | 8811088 | stop gained | C/A;T | snv | 4.4E-05; 5.4E-06 | 0.700 | 0 | |||||||
|
9 | 0.827 | 0.160 | 1 | 155904739 | missense variant | C/A;G;T | snv | 0.700 | 0 | ||||||||
|
8 | 0.827 | 0.080 | 8 | 11750213 | missense variant | G/A;C;T | snv | 0.020 | 1.000 | 2 | 2012 | 2019 | |||||
|
3 | 0.925 | 0.040 | 9 | 131134988 | missense variant | A/G | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2012 | 2012 |