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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 112504257 | intron variant | C/A | snv | 7.8E-02 |
|
0.700 | 1.000 | 3 | 2018 | 2019 | ||||||||||
|
1 | 112501706 | intron variant | G/T | snv | 8.8E-02 |
|
0.700 | 1.000 | 2 | 2018 | 2018 | ||||||||||
|
1 | 112501706 | intron variant | G/T | snv | 8.8E-02 |
|
0.700 | 1.000 | 2 | 2018 | 2019 | ||||||||||
|
1 | 112504257 | intron variant | C/A | snv | 7.8E-02 |
|
0.700 | 1.000 | 2 | 2018 | 2018 | ||||||||||
|
1 | 112501706 | intron variant | G/T | snv | 8.8E-02 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1 | 112501706 | intron variant | G/T | snv | 8.8E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.925 | 0.040 | 1 | 112465599 | upstream gene variant | G/A;T | snv |
|
Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.040 | 1 | 112465599 | upstream gene variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1 | 112500200 | intron variant | T/C | snv | 8.6E-02 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1 | 112500200 | intron variant | T/C | snv | 8.6E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1 | 112481358 | intron variant | A/G | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1 | 112481358 | intron variant | A/G | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1 | 112521149 | 3 prime UTR variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
1 | 112502439 | intron variant | A/C;T | snv | 0.72 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1 | 112502439 | intron variant | A/C;T | snv | 0.72 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.120 | 1 | 112503773 | intron variant | T/C;G | snv |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1 | 112504257 | intron variant | C/A | snv | 7.8E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1 | 112504257 | intron variant | C/A | snv | 7.8E-02 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1 | 112504257 | intron variant | C/A | snv | 7.8E-02 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1 | 112509564 | intron variant | G/C | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1 | 112476560 | intron variant | C/T | snv | 3.3E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 112512314 | intron variant | T/G | snv | 7.0E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 112512314 | intron variant | T/G | snv | 7.0E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.882 | 0.160 | 1 | 112514896 | stop gained | C/A;T | snv | 1.6E-05; 1.2E-05 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 1 | 112514896 | stop gained | C/A;T | snv | 1.6E-05; 1.2E-05 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Mental Disorders | 0.700 | 0 |