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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.716 | 0.360 | 11 | 102842889 | missense variant | T/C | snv | 0.58 | 0.57 |
|
0.030 | 1.000 | 3 | 2009 | 2019 | |||||||
|
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 | ||||||||
|
0.716 | 0.360 | 11 | 102842889 | missense variant | T/C | snv | 0.58 | 0.57 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.020 | 1.000 | 2 | 2009 | 2009 | ||||||
|
0.716 | 0.360 | 11 | 102842889 | missense variant | T/C | snv | 0.58 | 0.57 |
|
Cardiovascular Diseases | 0.020 | 1.000 | 2 | 2009 | 2014 | ||||||
|
0.716 | 0.360 | 11 | 102842889 | missense variant | T/C | snv | 0.58 | 0.57 |
|
Cardiovascular Diseases | 0.020 | 1.000 | 2 | 2008 | 2014 | ||||||
|
0.716 | 0.360 | 11 | 102842889 | missense variant | T/C | snv | 0.58 | 0.57 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.020 | 0.500 | 2 | 2010 | 2018 | ||||||
|
1.000 | 0.040 | 11 | 102843480 | missense variant | C/T | snv | 4.0E-06 |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1.000 | 0.040 | 11 | 102835992 | 3 prime UTR variant | G/A | snv | 1.5E-02 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
11 | 102840709 | intron variant | C/T | snv | 2.1E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 102840709 | intron variant | C/T | snv | 2.1E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
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 | |||||||
|
1.000 | 0.040 | 11 | 102839976 | intron variant | T/A | snv | 0.11 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.040 | 11 | 102839976 | intron variant | T/A | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.040 | 11 | 102845095 | upstream gene variant | C/A | snv | 0.10 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.040 | 11 | 102845095 | upstream gene variant | C/A | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
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 | ||||||
|
0.763 | 0.320 | 11 | 102844317 | upstream gene variant | T/C | snv | 0.23 |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.763 | 0.320 | 11 | 102844317 | upstream gene variant | T/C | snv | 0.23 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.763 | 0.320 | 11 | 102844317 | upstream gene variant | T/C | snv | 0.23 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.763 | 0.320 | 11 | 102844317 | upstream gene variant | T/C | snv | 0.23 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.763 | 0.320 | 11 | 102844317 | upstream gene variant | T/C | snv | 0.23 |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.763 | 0.320 | 11 | 102844317 | upstream gene variant | T/C | snv | 0.23 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.763 | 0.320 | 11 | 102844317 | upstream gene variant | T/C | snv | 0.23 |
|
Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 |