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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 |
|
Infections | 0.070 | 1.000 | 7 | 2010 | 2018 | |||||||
|
0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 |
|
Infections | 0.040 | 0.750 | 4 | 2011 | 2019 | |||||||
|
0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 |
|
Infections | 0.040 | 1.000 | 4 | 2008 | 2014 | |||||||
|
0.776 | 0.280 | 19 | 7747650 | upstream gene variant | A/G;T | snv | 0.66 |
|
Infections; Nervous System Diseases | 0.020 | 1.000 | 2 | 2012 | 2017 | |||||||
|
0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 |
|
Digestive System Diseases; Infections | 0.020 | 1.000 | 2 | 2010 | 2012 | |||||||
|
0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 |
|
Infections | 0.020 | 1.000 | 2 | 2012 | 2014 | |||||||
|
1.000 | 0.080 | 19 | 7745120 | intron variant | G/A | snv | 6.5E-02 | 6.3E-02 |
|
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.776 | 0.280 | 19 | 7747650 | upstream gene variant | A/G;T | snv | 0.66 |
|
Infections | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.776 | 0.280 | 19 | 7747650 | upstream gene variant | A/G;T | snv | 0.66 |
|
Infections | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.776 | 0.280 | 19 | 7747650 | upstream gene variant | A/G;T | snv | 0.66 |
|
Infections | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.776 | 0.280 | 19 | 7747650 | upstream gene variant | A/G;T | snv | 0.66 |
|
Digestive System Diseases; Infections | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.776 | 0.280 | 19 | 7747650 | upstream gene variant | A/G;T | snv | 0.66 |
|
Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.776 | 0.280 | 19 | 7747650 | upstream gene variant | A/G;T | snv | 0.66 |
|
Nervous System Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.776 | 0.280 | 19 | 7747650 | upstream gene variant | A/G;T | snv | 0.66 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.776 | 0.280 | 19 | 7747650 | upstream gene variant | A/G;T | snv | 0.66 |
|
Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.882 | 0.080 | 19 | 7744967 | missense variant | C/T | snv | 2.0E-05 | 2.1E-05 |
|
Infections | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
|
0.882 | 0.080 | 19 | 7744967 | missense variant | C/T | snv | 2.0E-05 | 2.1E-05 |
|
Infections | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
|
0.882 | 0.080 | 19 | 7744967 | missense variant | C/T | snv | 2.0E-05 | 2.1E-05 |
|
Infections; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
|
1.000 | 0.080 | 19 | 7740242 | 3 prime UTR variant | G/A | snv | 0.81 |
|
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 |
|
Infections | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 |
|
Digestive System Diseases; Infections | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 |
|
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 |
|
Infections | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 |
|
Digestive System Diseases | 0.010 | < 0.001 | 1 | 2007 | 2007 |