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 | 0.742 | 0.320 | 12 | 112450398 | missense variant | C/T | snv | 0.730 | 1.000 | 3 | 2004 | 2014 | |||||
|
25 | 0.708 | 0.440 | 12 | 112450406 | missense variant | G/A;C | snv | 0.870 | 1.000 | 10 | 2003 | 2019 | |||||
|
7 | 0.827 | 0.200 | 12 | 112450407 | missense variant | A/C;G;T | snv | 0.800 | 1.000 | 13 | 2003 | 2016 | |||||
|
14 | 0.752 | 0.280 | 12 | 112450416 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 5 | 143041855 | missense variant | A/C;G | snv | 4.3E-06; 4.3E-06 | 0.800 | 1.000 | 1 | 2014 | 2014 | ||||
|
1 | 1.000 | 0.080 | 22 | 30889607 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 0.010 | 1.000 | 1 | 2019 | 2019 | |||
|
10 | 0.790 | 0.360 | 17 | 31258500 | missense variant | A/C;G | snv | 0.700 | 0 | ||||||||
|
7 | 0.807 | 0.280 | 17 | 31334927 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.160 | 17 | 31261810 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
5 | 0.827 | 0.280 | 17 | 31235729 | missense variant | G/A;C | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 8 | 122951616 | missense variant | G/A;T | snv | 8.8E-05 | 3.5E-05 | 0.010 | 1.000 | 1 | 2012 | 2012 | |||
|
5 | 0.827 | 0.280 | 17 | 31335032 | splice donor variant | G/A | snv | 0.700 | 0 | ||||||||
|
5 | 0.827 | 0.280 | 17 | 31227232 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
5 | 0.827 | 0.280 | 17 | 31260481 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
27 | 0.672 | 0.400 | 12 | 25227341 | missense variant | T/A;G | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.160 | 17 | 31221842 | splice region variant | A/G | snv | 0.700 | 0 | ||||||||
|
9 | 0.807 | 0.240 | 11 | 119278181 | missense variant | T/A;C | snv | 8.0E-06 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
5 | 0.851 | 0.320 | 18 | 44951942 | missense variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
15 | 0.752 | 0.400 | 12 | 112477719 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 0.700 | 0 | ||||||
|
5 | 0.827 | 0.080 | 11 | 119278182 | missense variant | A/C;G | snv | 0.710 | 1.000 | 1 | 2015 | 2015 | |||||
|
5 | 0.827 | 0.240 | 12 | 112450352 | missense variant | A/C;G;T | snv | 0.700 | 0 | ||||||||
|
6 | 0.807 | 0.240 | 12 | 112450354 | missense variant | C/A;G | snv | 0.700 | 0 | ||||||||
|
8 | 0.776 | 0.280 | 12 | 112450361 | missense variant | G/A;C;T | snv | 0.810 | 1.000 | 22 | 2003 | 2017 | |||||
|
3 | 0.882 | 0.240 | 12 | 112450385 | missense variant | G/A;C | snv | 0.800 | 1.000 | 2 | 2003 | 2016 | |||||
|
10 | 0.790 | 0.240 | 12 | 112450408 | missense variant | G/C;T | snv | 0.700 | 0 |