Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
4 | 105404743 | intron variant | C/T | snv | 0.47 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 2 | 2018 | 2018 | |||||||||
|
4 | 105436974 | intron variant | C/G | snv | 3.4E-03 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
4 | 105391656 | intron variant | T/C | snv | 0.26 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
4 | 105398679 | non coding transcript exon variant | T/G | snv | 0.42 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
4 | 105395270 | intron variant | C/T | snv | 0.26 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
4 | 105466947 | intron variant | G/A | snv | 8.0E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.080 | 4 | 105435604 | intron variant | C/A | snv | 0.21 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 4 | 105386625 | missense variant | T/G | snv |
|
0.800 | 0 | |||||||||||||
|
1.000 | 4 | 105449391 | missense variant | T/C | snv |
|
0.800 | 0 | |||||||||||||
|
1.000 | 4 | 105449353 | missense variant | C/A | snv |
|
0.800 | 0 | |||||||||||||
|
1.000 | 4 | 105456721 | missense variant | G/A;C | snv | 8.1E-06; 4.0E-06 |
|
0.700 | 0 | ||||||||||||
|
1.000 | 4 | 105437978 | missense variant | G/A | snv | 1.6E-05 |
|
0.800 | 1.000 | 2 | 2016 | 2016 | |||||||||
|
1.000 | 4 | 105446444 | missense variant | C/A;T | snv | 1.5E-04; 2.0E-05 |
|
0.800 | 1.000 | 2 | 2016 | 2016 | |||||||||
|
1.000 | 4 | 105399137 | missense variant | G/A | snv | 2.0E-04 | 4.3E-04 |
|
0.700 | 0 | |||||||||||
|
0.925 | 4 | 105437964 | missense variant | C/T | snv | 4.9E-04 | 6.9E-04 |
|
0.800 | 1.000 | 2 | 2016 | 2016 | ||||||||
|
0.925 | 4 | 105437964 | missense variant | C/T | snv | 4.9E-04 | 6.9E-04 |
|
0.800 | 1.000 | 1 | 2016 | 2016 |