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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | 0.700 | 0 | |||||||||||
|
0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv |
|
Behavior and Behavior Mechanisms | 0.700 | 0 | |||||||||||
|
0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.700 | 0 | |||||||||||
|
0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv |
|
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | 0.700 | 0 | |||||||||||
|
0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv |
|
Musculoskeletal Diseases | 0.700 | 0 | |||||||||||
|
0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases | 0.700 | 0 | |||||||||||
|
0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv |
|
Otorhinolaryngologic Diseases | 0.700 | 0 | |||||||||||
|
0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv |
|
0.800 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
5 | 157345966 | intron variant | C/A | snv | 0.22 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
5 | 157327243 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
1.000 | 5 | 157294835 | missense variant | G/C;T | snv |
|
0.800 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
5 | 157316075 | intron variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
1.000 | 0.120 | 5 | 157269485 | 5 prime UTR variant | C/A;G | snv | 0.46 |
|
Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 |