| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
7 | 100022093 | intron variant | T/A | snv | 6.9E-03 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
7 | 100108776 | 3 prime UTR variant | C/G | snv | 1.1E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
14 | 100134466 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
2 | 100147663 | intron variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
7 | 100219573 | 3 prime UTR variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
7 | 100614631 | intron variant | G/A;C | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
7 | 100616392 | downstream gene variant | A/G | snv | 0.22 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
7 | 100624226 | intron variant | C/T | snv | 0.69 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
7 | 100637885 | intron variant | G/A | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.851 | 0.120 | 7 | 100638347 | intron variant | C/A | snv | 0.65 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
14 | 100710432 | regulatory region variant | G/A | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
7 | 100743255 | intron variant | C/T | snv | 1.9E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
7 | 100816525 | intron variant | G/A | snv | 1.6E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
7 | 100834812 | intron variant | G/A | snv | 1.2E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
7 | 101111694 | intergenic variant | G/A | snv | 0.96 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
7 | 101219111 | non coding transcript exon variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
3 | 101417558 | intron variant | G/A;C | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
3 | 101442847 | intron variant | A/-;AA;AAA | delins |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
10 | 101503499 | intron variant | C/T | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
7 | 101767398 | intergenic variant | C/T | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
10 | 102125800 | intergenic variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
10 | 102142302 | intron variant | AT/-;ATAT | delins |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
8 | 102239027 | upstream gene variant | C/A | snv | 2.8E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 102284277 | intron variant | A/G | snv | 1.6E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
14 | 102304810 | intron variant | C/T | snv | 4.5E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |