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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.807 | 0.360 | 16 | 11144926 | intron variant | G/A | snv | 0.33 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.840 | 1.000 | 4 | 2007 | 2010 | |||||||
|
0.925 | 0.160 | 16 | 11096031 | intron variant | T/C | snv | 0.51 |
|
Skin and Connective Tissue Diseases; Immune System Diseases | 0.810 | 1.000 | 2 | 2011 | 2013 | |||||||
|
0.807 | 0.320 | 16 | 11086016 | intron variant | A/G | snv | 0.37 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.800 | 1.000 | 5 | 2007 | 2011 | |||||||
|
0.882 | 0.200 | 16 | 11093926 | intron variant | G/A | snv | 0.34 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.800 | 1.000 | 3 | 2011 | 2015 | |||||||
|
0.882 | 0.240 | 16 | 11100914 | intron variant | C/A;T | snv | 0.29 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.800 | 1.000 | 2 | 2011 | 2015 | |||||||
|
1.000 | 0.080 | 16 | 11072831 | intron variant | C/A | snv | 0.40 |
|
Immune System Diseases; Nervous System Diseases | 0.800 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1.000 | 0.080 | 16 | 11083967 | intron variant | C/T | snv | 0.39 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.800 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.882 | 0.200 | 16 | 11083944 | intron variant | A/G | snv | 0.59 |
|
Immune System Diseases; Nervous System Diseases | 0.800 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.080 | 16 | 11136846 | intron variant | T/C | snv | 0.23 |
|
Immune System Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.851 | 0.240 | 16 | 11075826 | intron variant | T/G | snv | 0.42 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.740 | 1.000 | 4 | 2007 | 2013 | |||||||
|
0.882 | 0.160 | 16 | 11003622 | intron variant | C/G;T | snv |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.730 | 1.000 | 4 | 2009 | 2011 | ||||||||
|
0.807 | 0.320 | 16 | 11086016 | intron variant | A/G | snv | 0.37 |
|
Immune System Diseases; Nervous System Diseases | 0.710 | 1.000 | 2 | 2011 | 2011 | |||||||
|
1.000 | 0.120 | 16 | 11148049 | intron variant | A/G | snv | 0.18 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.710 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.925 | 0.120 | 16 | 11134855 | intron variant | C/T | snv | 0.18 |
|
Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases | 0.710 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.120 | 16 | 11134855 | intron variant | C/T | snv | 0.18 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.710 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1.000 | 0.080 | 16 | 11080508 | intron variant | G/A | snv | 0.34 |
|
Skin and Connective Tissue Diseases; Immune System Diseases | 0.700 | 1.000 | 3 | 2015 | 2017 | |||||||
|
1.000 | 0.120 | 16 | 11183501 | downstream gene variant | C/T | snv | 0.39 |
|
Immune System Diseases | 0.700 | 1.000 | 2 | 2016 | 2017 | |||||||
|
1.000 | 0.080 | 16 | 11116590 | intron variant | G/A | snv | 0.34 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 1.000 | 2 | 2011 | 2012 | |||||||
|
0.882 | 0.120 | 16 | 11119164 | intron variant | T/A | snv | 0.19 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 2 | 2019 | 2019 | |||||||
|
1.000 | 0.080 | 16 | 11136846 | intron variant | T/C | snv | 0.23 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 2 | 2016 | 2019 | |||||||
|
1.000 | 0.120 | 16 | 11183501 | downstream gene variant | C/T | snv | 0.39 |
|
Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.080 | 16 | 11129597 | intron variant | C/A;G | snv | 0.48 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.080 | 16 | 11129597 | intron variant | C/A;G | snv | 0.48 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.080 | 16 | 11071160 | intron variant | T/C | snv | 0.41 |
|
Immune System Diseases; Nervous System Diseases | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.925 | 0.160 | 16 | 11096031 | intron variant | T/C | snv | 0.51 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2007 | 2007 |