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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.882 | 0.240 | 14 | 96204802 | 5 prime UTR variant | C/T | snv | 0.41 | 0.39 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||||
|
0.882 | 0.040 | 14 | 96204324 | upstream gene variant | T/C | snv | 0.78 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.882 | 0.040 | 14 | 96204324 | upstream gene variant | T/C | snv | 0.78 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.882 | 0.040 | 14 | 96204324 | upstream gene variant | T/C | snv | 0.78 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.882 | 0.040 | 14 | 96204324 | upstream gene variant | T/C | snv | 0.78 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.882 | 0.040 | 14 | 96204324 | upstream gene variant | T/C | snv | 0.78 |
|
Behavior and Behavior Mechanisms | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.882 | 0.240 | 14 | 96204802 | 5 prime UTR variant | C/T | snv | 0.41 | 0.39 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
|
14 | 96222623 | intron variant | A/C | snv | 0.54 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
14 | 96222430 | intron variant | C/T | snv | 0.54 |
|
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
14 | 96209596 | intron variant | A/C;G;T | snv |
|
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
0.882 | 0.240 | 14 | 96204802 | 5 prime UTR variant | C/T | snv | 0.41 | 0.39 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.925 | 0.120 | 14 | 96242445 | 3 prime UTR variant | A/T | snv | 0.27 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.120 | 14 | 96242445 | 3 prime UTR variant | A/T | snv | 0.27 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.882 | 0.240 | 14 | 96204802 | 5 prime UTR variant | C/T | snv | 0.41 | 0.39 |
|
Behavior and Behavior Mechanisms | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
|
14 | 96214520 | intron variant | A/C | snv | 1.2E-03 |
|
Digestive System Diseases; Chemically-Induced Disorders | 0.010 | 1.000 | 1 | 2019 | 2019 |