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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
11 | 45206016 | intron variant | C/T | snv | 0.21 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
11 | 45230309 | 3 prime UTR variant | C/A;G | snv | 0.56 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
11 | 45160131 | intron variant | C/T | snv | 0.30 |
|
Infections | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
11 | 45223352 | intron variant | C/G | snv | 0.70 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
11 | 45223352 | intron variant | C/G | snv | 0.70 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 11 | 45216307 | intron variant | T/A;G | snv |
|
Endocrine System Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 11 | 45179068 | intron variant | G/A;C | snv |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
11 | 45206016 | intron variant | C/T | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
11 | 45229181 | 3 prime UTR variant | A/C | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||||
|
11 | 45234375 | 3 prime UTR variant | C/T | snv | 0.60 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
11 | 45101435 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
0.925 | 0.120 | 11 | 45204720 | missense variant | A/G | snv | 1.8E-03 | 1.8E-03 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 0 | |||||||||
|
0.925 | 0.120 | 11 | 45204720 | missense variant | A/G | snv | 1.8E-03 | 1.8E-03 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 0 | |||||||||
|
0.925 | 0.120 | 11 | 45224227 | missense variant | G/A;T | snv | 1.5E-04; 8.2E-02 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 0 | ||||||||||
|
0.925 | 0.120 | 11 | 45224227 | missense variant | G/A;T | snv | 1.5E-04; 8.2E-02 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 0 |