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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.080 | 3 | 141556594 | intron variant | G/T | snv | 6.7E-02 |
|
0.700 | 1.000 | 6 | 2015 | 2019 | ||||||||
|
3 | 141487958 | intron variant | C/T | snv | 4.7E-02 |
|
0.700 | 1.000 | 2 | 2016 | 2019 | ||||||||||
|
3 | 141602994 | intron variant | -/CT | delins | 0.29 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
3 | 141614997 | 3 prime UTR variant | C/T | snv | 4.8E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
3 | 141605663 | intron variant | C/A;G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
3 | 141576208 | intron variant | A/G | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
3 | 141488733 | intron variant | G/A | snv | 0.55 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.925 | 0.080 | 3 | 141556594 | intron variant | G/T | snv | 6.7E-02 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
3 | 141587171 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
3 | 141587171 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
3 | 141607760 | splice region variant | T/C | snv | 0.12 | 0.13 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
3 | 141497704 | intron variant | AAAAAA/-;AAAA;AAAAA;AAAAAAA | delins |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
3 | 141576936 | intron variant | T/A | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
3 | 141576936 | intron variant | T/A | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
3 | 141561431 | intron variant | T/C | snv | 6.7E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.080 | 3 | 141547651 | intron variant | G/A | snv | 0.55 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 3 | 141547651 | intron variant | G/A | snv | 0.55 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 3 | 141547651 | intron variant | G/A | snv | 0.55 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
3 | 141499112 | intron variant | T/C | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
3 | 141513090 | intron variant | G/A | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
3 | 141571742 | intron variant | C/A | snv | 1.3E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
3 | 141529673 | intron variant | A/C;G | snv | 4.8E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
3 | 141529673 | intron variant | A/C;G | snv | 4.8E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
3 | 141532813 | intron variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
3 | 141487958 | intron variant | C/T | snv | 4.7E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 |