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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.040 | 15 | 84037709 | missense variant | C/T | snv | 0.22 | 0.19 |
|
Mental Disorders | 0.800 | 1.000 | 5 | 2009 | 2019 | ||||||
|
15 | 83899406 | intron variant | T/A | snv | 0.63 |
|
0.700 | 1.000 | 3 | 2008 | 2019 | ||||||||||
|
15 | 83913372 | missense variant | G/A;T | snv | 1.6E-05; 0.61 |
|
0.700 | 1.000 | 3 | 2009 | 2019 | ||||||||||
|
15 | 83899406 | intron variant | T/A | snv | 0.63 |
|
0.700 | 1.000 | 2 | 2008 | 2010 | ||||||||||
|
15 | 83911404 | intron variant | G/A | snv | 0.63 |
|
0.700 | 1.000 | 2 | 2013 | 2019 | ||||||||||
|
15 | 83911830 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 2 | 2010 | 2019 | |||||||||||
|
15 | 83888924 | intron variant | T/G | snv | 0.62 |
|
0.700 | 1.000 | 2 | 2015 | 2019 | ||||||||||
|
15 | 83913372 | missense variant | G/A;T | snv | 1.6E-05; 0.61 |
|
0.700 | 1.000 | 2 | 2009 | 2010 | ||||||||||
|
15 | 83904289 | intron variant | T/G | snv | 0.63 |
|
0.700 | 1.000 | 2 | 2010 | 2019 | ||||||||||
|
1.000 | 0.040 | 15 | 83724155 | intron variant | G/A | snv | 0.84 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
15 | 83916786 | intron variant | -/TAAA | delins |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
15 | 83911404 | intron variant | G/A | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
15 | 83911830 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||||
|
15 | 83946227 | intron variant | G/C | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 83769541 | intron variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
15 | 83907596 | intron variant | G/A | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 83854003 | intron variant | C/T | snv | 0.32 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
15 | 83854003 | intron variant | C/T | snv | 0.32 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
15 | 83915207 | intron variant | T/C | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1.000 | 0.040 | 15 | 84039099 | 3 prime UTR variant | A/G | snv | 0.19 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
15 | 83920861 | intron variant | T/G | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 83678999 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
1.000 | 0.040 | 15 | 83847191 | intron variant | C/G | snv | 7.0E-02 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
15 | 83913372 | missense variant | G/A;T | snv | 1.6E-05; 0.61 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
15 | 83918855 | intron variant | C/T | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2017 | 2017 |