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 | 122194347 | intron variant | A/G | snv | 0.11 |
|
Digestive System Diseases; Nutritional and Metabolic Diseases | 0.800 | 1.000 | 3 | 2007 | 2014 | |||||||
|
0.807 | 0.280 | 4 | 122297158 | intron variant | A/G | snv | 0.10 |
|
Digestive System Diseases | 0.020 | 1.000 | 2 | 2009 | 2009 | |||||||
|
0.807 | 0.280 | 4 | 122297158 | intron variant | A/G | snv | 0.10 |
|
Digestive System Diseases | 0.710 | 1.000 | 2 | 2011 | 2012 | |||||||
|
0.807 | 0.280 | 4 | 122297158 | intron variant | A/G | snv | 0.10 |
|
Digestive System Diseases; Nutritional and Metabolic Diseases | 0.710 | 1.000 | 2 | 2007 | 2008 | |||||||
|
0.827 | 0.200 | 4 | 122194347 | intron variant | A/G | snv | 0.11 |
|
Immune System Diseases | 0.710 | 1.000 | 2 | 2010 | 2011 | |||||||
|
1.000 | 4 | 122249571 | missense variant | G/A | snv |
|
0.800 | 1.000 | 2 | 2015 | 2018 | ||||||||||
|
1.000 | 4 | 122309365 | missense variant | G/C | snv |
|
0.800 | 1.000 | 2 | 2015 | 2018 | ||||||||||
|
1.000 | 4 | 122243045 | missense variant | G/A;C | snv | 1.6E-05; 4.0E-06 |
|
0.700 | 1.000 | 2 | 2015 | 2018 | |||||||||
|
0.776 | 0.400 | 4 | 122211337 | intron variant | A/G | snv | 0.29 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.020 | 1.000 | 2 | 2009 | 2020 | |||||||
|
0.925 | 0.120 | 4 | 122219915 | intron variant | T/C | snv | 6.5E-02 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 2 | 2019 | 2019 | |||||||
|
0.925 | 0.040 | 4 | 122240464 | intron variant | A/G | snv | 0.24 |
|
Digestive System Diseases | 0.800 | 1.000 | 2 | 2012 | 2015 | |||||||
|
4 | 122359705 | synonymous variant | T/C | snv | 0.19 | 0.17 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.080 | 4 | 122306958 | intron variant | T/C | snv | 0.25 |
|
Digestive System Diseases; Nutritional and Metabolic Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.882 | 0.120 | 4 | 122151854 | upstream gene variant | T/C | snv | 0.24 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.882 | 0.120 | 4 | 122151854 | upstream gene variant | T/C | snv | 0.24 |
|
Digestive System Diseases; Nutritional and Metabolic Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.882 | 0.120 | 4 | 122151854 | upstream gene variant | T/C | snv | 0.24 |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.807 | 0.280 | 4 | 122297158 | intron variant | A/G | snv | 0.10 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.800 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.807 | 0.280 | 4 | 122297158 | intron variant | A/G | snv | 0.10 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.807 | 0.280 | 4 | 122297158 | intron variant | A/G | snv | 0.10 |
|
Neoplasms; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.807 | 0.280 | 4 | 122297158 | intron variant | A/G | snv | 0.10 |
|
Neoplasms; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.807 | 0.280 | 4 | 122297158 | intron variant | A/G | snv | 0.10 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.827 | 0.200 | 4 | 122194347 | intron variant | A/G | snv | 0.11 |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.827 | 0.200 | 4 | 122194347 | intron variant | A/G | snv | 0.11 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.827 | 0.200 | 4 | 122194347 | intron variant | A/G | snv | 0.11 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.827 | 0.200 | 4 | 122194347 | intron variant | A/G | snv | 0.11 |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 |