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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
3 | 49100471 | intron variant | G/T | snv | 0.74 | 0.66 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Eye Diseases; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Mental Disorders | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Nervous System Diseases; Mental Disorders | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Mental Disorders | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Eye Diseases; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Nervous System Diseases; Mental Disorders | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.120 | 3 | 49104420 | missense variant | A/G | snv | 4.0E-06 |
|
0.800 | 1.000 | 2 | 2014 | 2016 | ||||||||
|
0.925 | 0.120 | 3 | 49104420 | missense variant | A/G | snv | 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 |