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 | 7 | 103635498 | missense variant | G/T | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 7 | 103503158 | missense variant | C/A;T | snv | 4.0E-06 |
|
0.700 | 0 | ||||||||||||
|
1.000 | 7 | 103636250 | missense variant | T/C | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 7 | 103490747 | missense variant | C/T | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 7 | 103630111 | missense variant | G/A | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.080 | 7 | 103917082 | frameshift variant | -/A | delins | 1.6E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
1.000 | 0.080 | 7 | 103557992 | stop gained | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 7 | 103553659 | splice donor variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.925 | 0.040 | 7 | 103545430 | intron variant | C/A | snv | 0.32 |
|
Mental Disorders | 0.020 | 1.000 | 2 | 2010 | 2011 | |||||||
|
0.925 | 0.080 | 7 | 103748638 | intron variant | T/A;C | snv |
|
Nervous System Diseases; Mental Disorders | 0.020 | 1.000 | 2 | 2015 | 2016 | ||||||||
|
1.000 | 0.080 | 7 | 103749507 | splice region variant | A/G | snv | 0.49 | 0.50 |
|
Nervous System Diseases; Mental Disorders | 0.020 | 1.000 | 2 | 2008 | 2015 | ||||||
|
1.000 | 0.040 | 7 | 103936441 | intron variant | T/C;G | snv |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 7 | 103540259 | missense variant | G/A | snv | 4.0E-06 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 7 | 103540259 | missense variant | G/A | snv | 4.0E-06 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 7 | 103989335 | missense variant | G/A;C | snv | 5.0E-06; 5.0E-06 |
|
Nervous System Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.120 | 7 | 103651777 | synonymous variant | T/C | snv | 7.5E-02 | 9.5E-02 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders | 0.010 | < 0.001 | 1 | 2018 | 2018 | ||||||
|
1.000 | 0.080 | 7 | 103669375 | intron variant | A/G | snv | 0.53 |
|
Nervous System Diseases; Mental Disorders | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1.000 | 0.040 | 7 | 103785668 | intron variant | A/T | snv | 0.67 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
7 | 103471538 | intron variant | T/C | snv | 0.45 |
|
Behavior and Behavior Mechanisms | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.882 | 0.120 | 7 | 103610714 | missense variant | G/A;C;T | snv | 1.2E-05; 0.12 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.882 | 0.120 | 7 | 103610714 | missense variant | G/A;C;T | snv | 1.2E-05; 0.12 |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.882 | 0.120 | 7 | 103610714 | missense variant | G/A;C;T | snv | 1.2E-05; 0.12 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.040 | 7 | 103545430 | intron variant | C/A | snv | 0.32 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.925 | 0.120 | 7 | 103539148 | synonymous variant | A/G | snv | 3.8E-02 | 2.1E-02 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders | 0.010 | < 0.001 | 1 | 2018 | 2018 | ||||||
|
0.925 | 0.120 | 7 | 103539148 | synonymous variant | A/G | snv | 3.8E-02 | 2.1E-02 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2019 | 2019 |