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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
20 | 53605567 | intron variant | C/T | snv | 8.1E-03 |
|
0.700 | 1.000 | 2 | 2016 | 2019 | ||||||||||
|
20 | 53605567 | intron variant | C/T | snv | 8.1E-03 |
|
0.700 | 1.000 | 2 | 2016 | 2019 | ||||||||||
|
20 | 53605567 | intron variant | C/T | snv | 8.1E-03 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
20 | 53591817 | intron variant | G/A | snv | 0.86 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.040 | 20 | 53595734 | intron variant | G/A | snv | 0.79 |
|
Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
20 | 53590524 | intron variant | T/C | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
20 | 53590524 | intron variant | T/C | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.080 | 20 | 53581860 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 |
|
Digestive System Diseases; Neoplasms | 0.700 | 0 | |||||||||
|
0.925 | 0.080 | 20 | 53567166 | 3 prime UTR variant | C/A;T | snv | 8.8E-02 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.925 | 0.080 | 20 | 53567166 | 3 prime UTR variant | C/A;T | snv | 8.8E-02 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.882 | 0.040 | 20 | 53581801 | synonymous variant | T/A | snv | 0.11 | 8.8E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.882 | 0.040 | 20 | 53581801 | synonymous variant | T/A | snv | 0.11 | 8.8E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.882 | 0.040 | 20 | 53581801 | synonymous variant | T/A | snv | 0.11 | 8.8E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.882 | 0.040 | 20 | 53577121 | missense variant | G/A | snv | 3.4E-02 | 1.6E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.882 | 0.040 | 20 | 53577121 | missense variant | G/A | snv | 3.4E-02 | 1.6E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.882 | 0.040 | 20 | 53577121 | missense variant | G/A | snv | 3.4E-02 | 1.6E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 |