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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.040 | 17 | 7001742 | synonymous variant | T/C;G | snv | 0.59 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.925 | 0.040 | 17 | 7001742 | synonymous variant | T/C;G | snv | 0.59 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
1.000 | 0.040 | 17 | 6997526 | intron variant | C/A;G;T | snv |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.776 | 0.280 | 17 | 6999441 | missense variant | A/G | snv | 0.60 | 0.62 |
|
Neoplasms; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.776 | 0.280 | 17 | 6999441 | missense variant | A/G | snv | 0.60 | 0.62 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
|
0.776 | 0.280 | 17 | 6999441 | missense variant | A/G | snv | 0.60 | 0.62 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
0.776 | 0.280 | 17 | 6999441 | missense variant | A/G | snv | 0.60 | 0.62 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||
|
0.776 | 0.280 | 17 | 6999441 | missense variant | A/G | snv | 0.60 | 0.62 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
|
0.776 | 0.280 | 17 | 6999441 | missense variant | A/G | snv | 0.60 | 0.62 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
|
0.776 | 0.280 | 17 | 6999441 | missense variant | A/G | snv | 0.60 | 0.62 |
|
Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.776 | 0.280 | 17 | 6999441 | missense variant | A/G | snv | 0.60 | 0.62 |
|
Neoplasms; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.925 | 0.160 | 17 | 6996757 | intron variant | G/A | snv | 0.20 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.925 | 0.160 | 17 | 6996757 | intron variant | G/A | snv | 0.20 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.010 | < 0.001 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.080 | 17 | 7003751 | intron variant | A/G | snv | 0.68 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1.000 | 0.120 | 17 | 7010333 | synonymous variant | G/A | snv | 0.11 | 8.8E-02 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections; Nervous System Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.925 | 0.160 | 17 | 7001615 | missense variant | A/C;G | snv | 4.0E-06; 0.38 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections; Nervous System Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.160 | 17 | 7001615 | missense variant | A/C;G | snv | 4.0E-06; 0.38 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 |