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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
7 | 0.925 | 21 | 37490393 | missense variant | C/T | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
45 | 0.708 | 0.440 | 19 | 1242559 | missense variant | C/T | snv | 6.7E-06 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
60 | 0.689 | 0.400 | 6 | 42978878 | stop gained | C/T | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
16 | 0.763 | 0.360 | 16 | 68329105 | stop gained | G/C;T | snv | 4.0E-06; 1.6E-05 | 0.700 | 0 | |||||||
|
33 | 0.752 | 0.400 | 5 | 60927745 | intron variant | C/A;G;T | snv | 0.700 | 0 | ||||||||
|
7 | 0.925 | 0.120 | 8 | 115604739 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.120 | 3 | 48567190 | missense variant | C/A;T | snv | 0.700 | 0 | ||||||||
|
16 | 0.732 | 0.320 | 20 | 58891811 | stop gained | C/G;T | snv | 0.700 | 0 | ||||||||
|
6 | 0.882 | 0.120 | 12 | 47984112 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.040 | 19 | 38499718 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
7 | 0.851 | 0.280 | 2 | 1484815 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.080 | 9 | 35801153 | stop gained | C/T | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
8 | 0.882 | X | 110264571 | stop gained | G/A | snv | 0.700 | 0 | |||||||||
|
7 | 0.882 | 0.200 | 3 | 47846550 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.120 | 14 | 78709310 | missense variant | A/G | snv | 1.4E-05 | 0.700 | 0 | |||||||
|
11 | 0.827 | 0.240 | 22 | 41173768 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
34 | 0.716 | 0.400 | 19 | 13136099 | missense variant | C/A;T | snv | 0.700 | 0 | ||||||||
|
19 | 0.763 | 0.240 | 14 | 102002950 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
5 | 0.882 | 0.160 | 8 | 143818255 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
9 | 0.807 | 0.160 | 8 | 143817591 | splice donor variant | C/T | snv | 0.700 | 0 | ||||||||
|
8 | 0.807 | 0.200 | 15 | 48463123 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
9 | 0.851 | 0.240 | 2 | 100006808 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
9 | 0.851 | 0.040 | 7 | 66994210 | splice donor variant | A/C;G | snv | 4.0E-06; 3.9E-03 | 0.700 | 0 | |||||||
|
64 | 0.672 | 0.520 | 3 | 132675903 | missense variant | G/A;T | snv | 1.9E-03; 4.1E-06 | 0.700 | 0 | |||||||
|
19 | 0.827 | 0.240 | 1 | 11992659 | missense variant | C/T | snv | 0.700 | 0 |