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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
18 | 63897904 | intron variant | T/G | snv | 1.8E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
18 | 63897904 | intron variant | T/G | snv | 1.8E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.925 | 0.080 | 18 | 63909374 | intron variant | C/T | snv | 4.7E-02 |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.925 | 0.080 | 18 | 63909374 | intron variant | C/T | snv | 4.7E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.807 | 0.160 | 18 | 63903295 | missense variant | C/G | snv | 0.29 | 0.28 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
|
0.807 | 0.160 | 18 | 63903295 | missense variant | C/G | snv | 0.29 | 0.28 |
|
Immune System Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
|
0.807 | 0.160 | 18 | 63903295 | missense variant | C/G | snv | 0.29 | 0.28 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
|
0.807 | 0.160 | 18 | 63903295 | missense variant | C/G | snv | 0.29 | 0.28 |
|
Skin and Connective Tissue Diseases; Immune System Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
|
0.807 | 0.160 | 18 | 63903295 | missense variant | C/G | snv | 0.29 | 0.28 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
|
0.807 | 0.160 | 18 | 63903295 | missense variant | C/G | snv | 0.29 | 0.28 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
|
0.851 | 0.320 | 18 | 63901881 | stop gained | C/A;T | snv | 7.0E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | 0.020 | 0.500 | 2 | 2009 | 2015 | |||||||
|
0.851 | 0.320 | 18 | 63901881 | stop gained | C/A;T | snv | 7.0E-05 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2003 | 2003 | |||||||
|
0.851 | 0.320 | 18 | 63901881 | stop gained | C/A;T | snv | 7.0E-05 |
|
Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.851 | 0.320 | 18 | 63901881 | stop gained | C/A;T | snv | 7.0E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 1997 | 1997 |