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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.827 | 0.200 | 4 | 83320204 | intron variant | G/A;C | snv |
|
Immune System Diseases | 0.020 | 1.000 | 2 | 2010 | 2014 | ||||||||
|
0.851 | 0.160 | 4 | 83309466 | missense variant | T/C | snv | 0.78 | 0.80 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
|
0.851 | 0.160 | 4 | 83309466 | missense variant | T/C | snv | 0.78 | 0.80 |
|
Pathological Conditions, Signs and Symptoms; Neoplasms | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.851 | 0.160 | 4 | 83309466 | missense variant | T/C | snv | 0.78 | 0.80 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.851 | 0.160 | 4 | 83309466 | missense variant | T/C | snv | 0.78 | 0.80 |
|
0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.851 | 0.160 | 4 | 83309466 | missense variant | T/C | snv | 0.78 | 0.80 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
|
4 | 83309725 | intron variant | T/G | snv | 0.71 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.925 | 0.120 | 4 | 83303254 | intron variant | T/G | snv | 0.82 |
|
Digestive System Diseases; Infections | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.120 | 4 | 83303254 | intron variant | T/G | snv | 0.82 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.120 | 4 | 83300266 | intron variant | A/G | snv | 0.63 |
|
Digestive System Diseases; Infections | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.120 | 4 | 83300266 | intron variant | A/G | snv | 0.63 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.851 | 0.160 | 4 | 83310887 | missense variant | G/A | snv | 8.0E-06 |
|
0.010 | 1.000 | 1 | 2003 | 2003 | ||||||||
|
0.851 | 0.160 | 4 | 83310887 | missense variant | G/A | snv | 8.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.851 | 0.160 | 4 | 83310887 | missense variant | G/A | snv | 8.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.851 | 0.160 | 4 | 83310887 | missense variant | G/A | snv | 8.0E-06 |
|
Eye Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
4 | 83322396 | intron variant | A/G | snv | 0.18 | 0.18 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
0.882 | 0.080 | 4 | 83302560 | intron variant | C/T | snv | 0.63 |
|
Immune System Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.882 | 0.080 | 4 | 83302560 | intron variant | C/T | snv | 0.63 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.882 | 0.080 | 4 | 83302560 | intron variant | C/T | snv | 0.63 |
|
0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.040 | 4 | 83292466 | 3 prime UTR variant | A/G | snv | 0.71 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.827 | 0.200 | 4 | 83320204 | intron variant | G/A;C | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.827 | 0.200 | 4 | 83320204 | intron variant | G/A;C | snv |
|
Immune System Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.827 | 0.200 | 4 | 83320204 | intron variant | G/A;C | snv |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.827 | 0.200 | 4 | 83320204 | intron variant | G/A;C | snv |
|
0.010 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
0.827 | 0.200 | 4 | 83320204 | intron variant | G/A;C | snv |
|
Pathological Conditions, Signs and Symptoms; Neoplasms | 0.010 | 1.000 | 1 | 2012 | 2012 |