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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 21044589 | upstream gene variant | G/A | snv | 0.25 |
|
0.700 | 1.000 | 2 | 2012 | 2012 | ||||||||||
|
2 | 21044589 | upstream gene variant | G/A | snv | 0.25 |
|
0.700 | 1.000 | 2 | 2012 | 2012 | ||||||||||
|
2 | 21044589 | upstream gene variant | G/A | snv | 0.25 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.708 | 0.440 | 2 | 21009323 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.700 | 1.000 | 5 | 2008 | 2012 | |||||||
|
0.708 | 0.440 | 2 | 21009323 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.800 | 1.000 | 5 | 2007 | 2019 | |||||||
|
0.708 | 0.440 | 2 | 21009323 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.800 | 1.000 | 2 | 2007 | 2019 | |||||||
|
0.708 | 0.440 | 2 | 21009323 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.800 | 1.000 | 2 | 2009 | 2019 | |||||||
|
0.708 | 0.440 | 2 | 21009323 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.710 | 1.000 | 1 | 2011 | 2016 | |||||||
|
0.708 | 0.440 | 2 | 21009323 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.708 | 0.440 | 2 | 21009323 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.925 | 0.080 | 2 | 21028042 | missense variant | G/A | snv | 0.49 | 0.39 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.080 | 2 | 21028042 | missense variant | G/A | snv | 0.49 | 0.39 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.080 | 2 | 21028042 | missense variant | G/A | snv | 0.49 | 0.39 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 |
|
0.800 | 1.000 | 2 | 2012 | 2018 | ||||||||
|
0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | ||||||||
|
0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||
|
0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||
|
0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv |
|
0.800 | 1.000 | 2 | 2012 | 2019 | |||||||||
|
0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv |
|
0.800 | 1.000 | 2 | 2009 | 2019 | |||||||||
|
0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 2 | 2012 | 2012 | |||||||||
|
0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||||
|
0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 |