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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.040 | 11 | 102840850 | intron variant | C/G | snv | 0.11 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.040 | 11 | 102840850 | intron variant | C/G | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.080 | 11 | 102835973 | 3 prime UTR variant | C/T | snv | 2.0E-02 |
|
Nervous System Diseases; Mental Disorders | 0.010 | 1.000 | 1 | 2005 | 2005 | |||||||
|
0.851 | 0.080 | 11 | 102843046 | intron variant | G/A;C | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.851 | 0.080 | 11 | 102843046 | intron variant | G/A;C | snv |
|
Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.851 | 0.080 | 11 | 102843046 | intron variant | G/A;C | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.851 | 0.080 | 11 | 102843046 | intron variant | G/A;C | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.925 | 0.120 | 11 | 102838694 | synonymous variant | A/G | snv | 0.57 | 0.54 |
|
Nervous System Diseases; Mental Disorders | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||||
|
0.925 | 0.120 | 11 | 102838694 | synonymous variant | A/G | snv | 0.57 | 0.54 |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
0.925 | 0.120 | 11 | 102836574 | non coding transcript exon variant | G/A;T | snv | 0.12; 6.7E-06 | 0.10 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.925 | 0.120 | 11 | 102836574 | non coding transcript exon variant | G/A;T | snv | 0.12; 6.7E-06 | 0.10 |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
|
0.925 | 0.120 | 11 | 102836574 | non coding transcript exon variant | G/A;T | snv | 0.12; 6.7E-06 | 0.10 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.882 | 0.120 | 11 | 102836608 | non coding transcript exon variant | C/A | snv | 0.54 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.882 | 0.120 | 11 | 102836608 | non coding transcript exon variant | C/A | snv | 0.54 |
|
Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.882 | 0.120 | 11 | 102836608 | non coding transcript exon variant | C/A | snv | 0.54 |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.882 | 0.160 | 11 | 102840607 | intron variant | T/C | snv | 0.58 | 0.57 |
|
0.020 | 1.000 | 2 | 2009 | 2017 | |||||||
|
0.827 | 0.160 | 11 | 102838056 | intron variant | G/A | snv | 0.31 |
|
0.020 | 1.000 | 2 | 2009 | 2017 | ||||||||
|
0.882 | 0.160 | 11 | 102840607 | intron variant | T/C | snv | 0.58 | 0.57 |
|
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
|
0.882 | 0.160 | 11 | 102840607 | intron variant | T/C | snv | 0.58 | 0.57 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
|
0.827 | 0.160 | 11 | 102838056 | intron variant | G/A | snv | 0.31 |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.827 | 0.160 | 11 | 102838056 | intron variant | G/A | snv | 0.31 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.827 | 0.160 | 11 | 102838056 | intron variant | G/A | snv | 0.31 |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.827 | 0.160 | 11 | 102838056 | intron variant | G/A | snv | 0.31 |
|
Musculoskeletal Diseases; Wounds and Injuries | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.827 | 0.160 | 11 | 102838056 | intron variant | G/A | snv | 0.31 |
|
Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.763 | 0.320 | 11 | 102844317 | upstream gene variant | T/C | snv | 0.23 |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 |