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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.040 | 1 | 24966593 | upstream gene variant | T/C;G | snv |
|
0.800 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1.000 | 0.080 | 1 | 24935531 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1 | 24924339 | intron variant | C/T | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.080 | 1 | 24965206 | upstream gene variant | C/T | snv | 6.5E-03 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 1 | 24951485 | intron variant | C/G | snv | 2.3E-03 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.827 | 0.120 | 1 | 24964519 | missense variant | A/T | snv | 0.56 | 0.50 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.080 | 1 | 24924933 | intron variant | G/A | snv | 0.53 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 1 | 24924933 | intron variant | G/A | snv | 0.53 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 1 | 24927826 | intron variant | C/T | snv | 0.53 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.040 | 1 | 24966593 | upstream gene variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
0.776 | 0.240 | 1 | 24925432 | intron variant | A/T | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.776 | 0.240 | 1 | 24925432 | intron variant | A/T | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 1 | 24946532 | intron variant | G/A | snv | 5.1E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 1 | 24914625 | intron variant | A/G | snv | 0.53 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.827 | 0.120 | 1 | 24964519 | missense variant | A/T | snv | 0.56 | 0.50 |
|
0.020 | 0.500 | 2 | 2015 | 2017 | |||||||
|
0.851 | 0.160 | 1 | 24951491 | intron variant | C/T | snv | 0.48 |
|
0.010 | < 0.001 | 1 | 2015 | 2015 | ||||||||
|
0.851 | 0.160 | 1 | 24951491 | intron variant | C/T | snv | 0.48 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
0.851 | 0.160 | 1 | 24951491 | intron variant | C/T | snv | 0.48 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
0.851 | 0.160 | 1 | 24951491 | intron variant | C/T | snv | 0.48 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
1.000 | 0.040 | 1 | 24944081 | intron variant | T/C | snv | 0.64 |
|
0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.040 | 1 | 24917063 | intron variant | C/T | snv | 0.12 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
1.000 | 0.080 | 1 | 24917276 | intron variant | A/G | snv | 0.45 |
|
0.010 | < 0.001 | 1 | 2015 | 2015 | ||||||||
|
0.827 | 0.120 | 1 | 24964519 | missense variant | A/T | snv | 0.56 | 0.50 |
|
0.010 | < 0.001 | 1 | 2009 | 2009 | |||||||
|
0.827 | 0.120 | 1 | 24964519 | missense variant | A/T | snv | 0.56 | 0.50 |
|
0.010 | < 0.001 | 1 | 2009 | 2009 | |||||||
|
0.827 | 0.120 | 1 | 24964519 | missense variant | A/T | snv | 0.56 | 0.50 |
|
0.010 | 1.000 | 1 | 2019 | 2019 |