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 | 0.360 | 15 | 78943104 | intron variant | T/C | snv | 0.50 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.800 | 1.000 | 2 | 2008 | 2009 | |||||||
|
15 | 78936857 | intron variant | A/G | snv | 0.85 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.851 | 0.120 | 15 | 78944951 | missense variant | C/T | snv | 9.3E-02 | 7.8E-02 |
|
Nervous System Diseases; Mental Disorders | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
0.851 | 0.120 | 15 | 78944951 | missense variant | C/T | snv | 9.3E-02 | 7.8E-02 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
0.851 | 0.120 | 15 | 78944951 | missense variant | C/T | snv | 9.3E-02 | 7.8E-02 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
0.851 | 0.120 | 15 | 78944951 | missense variant | C/T | snv | 9.3E-02 | 7.8E-02 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1.000 | 0.120 | 15 | 78942615 | intron variant | G/A;C | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.120 | 15 | 78942615 | intron variant | G/A;C | snv | 0.10 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.827 | 0.360 | 15 | 78943104 | intron variant | T/C | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.827 | 0.360 | 15 | 78943104 | intron variant | T/C | snv | 0.50 |
|
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.827 | 0.360 | 15 | 78943104 | intron variant | T/C | snv | 0.50 |
|
Pathological Conditions, Signs and Symptoms; Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.827 | 0.360 | 15 | 78943104 | intron variant | T/C | snv | 0.50 |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.827 | 0.360 | 15 | 78943104 | intron variant | T/C | snv | 0.50 |
|
Immune System Diseases; Nervous System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
15 | 78938704 | intron variant | G/T | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
15 | 78938663 | intron variant | T/C | snv | 1.0E-01 |
|
0.700 | 1.000 | 1 | 2018 | 2018 |