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 | 0.160 | 19 | 10274864 | missense variant | A/G;T | snv | 4.0E-06; 2.8E-02 |
|
0.700 | 0 | |||||||||||
|
0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 |
|
Eye Diseases; Immune System Diseases; Endocrine System Diseases | 0.020 | < 0.001 | 2 | 2007 | 2013 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Eye Diseases; Immune System Diseases; Endocrine System Diseases | 0.020 | < 0.001 | 2 | 2007 | 2013 | ||||||
|
0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 |
|
Digestive System Diseases | 0.010 | < 0.001 | 1 | 2015 | 2015 | ||||||
|
0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 |
|
Digestive System Diseases | 0.010 | < 0.001 | 1 | 2004 | 2004 | ||||||
|
0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 |
|
Digestive System Diseases | 0.010 | < 0.001 | 1 | 2015 | 2015 | ||||||
|
0.851 | 0.280 | 19 | 10279982 | intron variant | C/G | snv | 0.52 |
|
Neoplasms | 0.010 | < 0.001 | 1 | 2016 | 2016 | |||||||
|
0.851 | 0.280 | 19 | 10279982 | intron variant | C/G | snv | 0.52 |
|
Neoplasms | 0.010 | < 0.001 | 1 | 2016 | 2016 | |||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Respiratory Tract Diseases; Cardiovascular Diseases | 0.010 | < 0.001 | 1 | 2019 | 2019 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.010 | < 0.001 | 1 | 2015 | 2015 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases | 0.010 | < 0.001 | 1 | 2005 | 2005 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | < 0.001 | 1 | 2013 | 2013 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases | 0.010 | < 0.001 | 1 | 2005 | 2005 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Cardiovascular Diseases | 0.010 | < 0.001 | 1 | 2004 | 2004 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | < 0.001 | 1 | 2013 | 2013 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases | 0.010 | < 0.001 | 1 | 2015 | 2015 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Pathological Conditions, Signs and Symptoms | 0.010 | < 0.001 | 1 | 2005 | 2005 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Immune System Diseases; Nervous System Diseases | 0.030 | 0.333 | 3 | 2003 | 2018 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases | 0.060 | 0.500 | 6 | 2006 | 2018 | ||||||
|
0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 |
|
Female Urogenital Diseases and Pregnancy Complications | 0.040 | 0.500 | 4 | 2003 | 2016 | ||||||
|
0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.020 | 0.500 | 2 | 2011 | 2016 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Nervous System Diseases | 0.020 | 0.500 | 2 | 2003 | 2005 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Nervous System Diseases; Mental Disorders | 0.020 | 0.500 | 2 | 2003 | 2003 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Digestive System Diseases | 0.020 | 0.500 | 2 | 2001 | 2015 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Cardiovascular Diseases | 0.020 | 0.500 | 2 | 2013 | 2015 |