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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.080 | 20 | 8789461 | intron variant | A/C | snv | 0.90 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 20 | 8753616 | intron variant | A/G | snv | 0.92 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
20 | 8635941 | intron variant | A/G | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.080 | 20 | 8785424 | intron variant | A/G | snv | 0.90 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
20 | 8334670 | intron variant | A/G | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
20 | 8330815 | intron variant | A/G | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.080 | 20 | 8769415 | intron variant | A/G;T | snv |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 20 | 8791897 | intron variant | A/G;T | snv |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
20 | 8628941 | intron variant | A/T | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
20 | 8628941 | intron variant | A/T | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1.000 | 0.080 | 20 | 8934668 | intron variant | A/T | snv | 0.30 |
|
Respiratory Tract Diseases; Nervous System Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
20 | 8645624 | intron variant | C/A | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
20 | 8148844 | intron variant | C/A | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 20 | 8348184 | intron variant | C/G | snv | 6.8E-03 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
20 | 8884359 | 3 prime UTR variant | C/T | snv | 0.56 |
|
Chemically-Induced Disorders; Mental Disorders | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.040 | 20 | 8790220 | missense variant | C/T | snv |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 20 | 8788533 | splice region variant | C/T | snv | 0.95 | 0.90 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
20 | 8623534 | intron variant | C/T | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 20 | 8733382 | frameshift variant | CTGT/- | delins |
|
0.700 | 0 | |||||||||||||
|
20 | 8626746 | intron variant | G/A | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
20 | 8626746 | intron variant | G/A | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
20 | 8626746 | intron variant | G/A | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
20 | 8626746 | intron variant | G/A | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1.000 | 0.040 | 20 | 8233139 | intron variant | G/A | snv | 0.34 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
20 | 8623946 | intron variant | G/A | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |