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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
7 | 34696590 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
7 | 34811812 | missense variant | A/C;G;T | snv | 4.0E-06; 2.3E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
0.700 | 0 | ||||||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Mental Disorders | 0.090 | 1.000 | 9 | 2011 | 2019 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Mental Disorders | 0.070 | 1.000 | 7 | 2011 | 2017 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Behavior and Behavior Mechanisms | 0.060 | 1.000 | 6 | 2011 | 2017 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.030 | 0.667 | 3 | 2006 | 2017 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Chemically-Induced Disorders; Mental Disorders | 0.020 | 1.000 | 2 | 2015 | 2016 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Mental Disorders | 0.020 | 1.000 | 2 | 2012 | 2013 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Mental Disorders | 0.020 | 0.500 | 2 | 2014 | 2015 | ||||||
|
1.000 | 0.120 | 7 | 34820377 | intron variant | G/C | snv | 0.14 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.925 | 7 | 34663912 | intron variant | G/A | snv | 4.2E-02 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.925 | 7 | 34663912 | intron variant | G/A | snv | 4.2E-02 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
7 | 34665211 | intron variant | A/G | snv | 0.56 |
|
Pathological Conditions, Signs and Symptoms | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
7 | 34709170 | intron variant | G/C | snv | 0.45 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
7 | 34716363 | intron variant | C/A | snv | 0.47 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Behavior and Behavior Mechanisms | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Behavior and Behavior Mechanisms | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Behavior and Behavior Mechanisms | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2013 | 2013 |