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 | X | 5903423 | frameshift variant | TC/- | delins |
|
0.700 | 0 | ||||||||||||
|
0.925 | 0.080 | X | 5903423 | frameshift variant | TC/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.925 | X | 5903492 | frameshift variant | -/A | delins |
|
0.700 | 0 | |||||||||||||
|
0.925 | X | 5903492 | frameshift variant | -/A | delins |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.080 | X | 5909225 | missense variant | C/T | snv | 1.6E-05 | 9.5E-06 |
|
Digestive System Diseases; Neoplasms | 0.700 | 0 | |||||||||
|
1.000 | X | 6151166 | stop gained | G/A | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.040 | X | 6227814 | 5 prime UTR variant | C/G;T | snv | 0.30 |
|
Mental Disorders | 0.010 | < 0.001 | 1 | 2008 | 2008 | |||||||
|
1.000 | 0.040 | X | 5903545 | missense variant | T/C | snv | 3.0E-04 | 2.8E-04 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
|
1.000 | 0.040 | X | 5890820 | 3 prime UTR variant | G/A | snv |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
1.000 | 0.040 | X | 6111492 | intron variant | A/G;T | snv |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.925 | 0.040 | X | 5893491 | missense variant | G/A;C;T | snv | 7.6E-03 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.040 | X | 5893489 | synonymous variant | G/A;C;T | snv | 1.2E-05; 6.7E-03 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.040 | X | 5893158 | missense variant | G/A | snv | 1.1E-05 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.040 | X | 5890820 | 3 prime UTR variant | G/A | snv |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.040 | X | 5892533 | 3 prime UTR variant | C/A;T | snv |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.040 | X | 5892643 | 3 prime UTR variant | G/T | snv | 0.11 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1.000 | 0.040 | X | 5892715 | 3 prime UTR variant | C/G;T | snv |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.040 | X | 5892258 | 3 prime UTR variant | G/A | snv | 0.15 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1.000 | 0.040 | X | 5894600 | intron variant | A/G | snv |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.040 | X | 6002841 | intron variant | A/G | snv | 0.28 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.080 | X | 6004425 | intron variant | A/G | snv | 0.28 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.925 | 0.040 | X | 5893158 | missense variant | G/A | snv | 1.1E-05 |
|
Mental Disorders | 0.020 | 1.000 | 2 | 2011 | 2019 | |||||||
|
0.925 | 0.040 | X | 5893491 | missense variant | G/A;C;T | snv | 7.6E-03 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.040 | X | 5893491 | missense variant | G/A;C;T | snv | 7.6E-03 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.040 | X | 5893489 | synonymous variant | G/A;C;T | snv | 1.2E-05; 6.7E-03 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2019 | 2019 |