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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
21 | 36074301 | intron variant | C/A | snv | 4.3E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.827 | 0.080 | 21 | 36074727 | intron variant | T/C | snv | 0.63 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.827 | 0.080 | 21 | 36074727 | intron variant | T/C | snv | 0.63 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.827 | 0.080 | 21 | 36074727 | intron variant | T/C | snv | 0.63 |
|
Neoplasms | 0.010 | < 0.001 | 1 | 2017 | 2017 | |||||||
|
0.827 | 0.080 | 21 | 36074727 | intron variant | T/C | snv | 0.63 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | < 0.001 | 1 | 2017 | 2017 | |||||||
|
0.827 | 0.080 | 21 | 36074727 | intron variant | T/C | snv | 0.63 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.827 | 0.080 | 21 | 36074727 | intron variant | T/C | snv | 0.63 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | < 0.001 | 1 | 2017 | 2017 | |||||||
|
0.851 | 0.080 | 21 | 36071595 | intron variant | T/C | snv | 0.74 |
|
Neoplasms | 0.010 | < 0.001 | 1 | 2017 | 2017 | |||||||
|
0.851 | 0.080 | 21 | 36071595 | intron variant | T/C | snv | 0.74 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.851 | 0.080 | 21 | 36071595 | intron variant | T/C | snv | 0.74 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.851 | 0.080 | 21 | 36071595 | intron variant | T/C | snv | 0.74 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.851 | 0.080 | 21 | 36071595 | intron variant | T/C | snv | 0.74 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
21 | 36049325 | intron variant | C/T | snv | 4.4E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.882 | 0.160 | 21 | 36073015 | 3 prime UTR variant | G/A | snv | 9.7E-02 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.882 | 0.160 | 21 | 36073015 | 3 prime UTR variant | G/A | snv | 9.7E-02 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.882 | 0.160 | 21 | 36073015 | 3 prime UTR variant | G/A | snv | 9.7E-02 |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 |