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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
8 | 107278644 | intron variant | G/A | snv | 0.78 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1.000 | 0.040 | 8 | 107266388 | intron variant | C/A | snv | 0.13 |
|
Eye Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
8 | 107276121 | intron variant | T/A | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
8 | 107405173 | intron variant | C/T | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
8 | 107388883 | intron variant | T/A | snv | 0.47 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
8 | 107276524 | intron variant | C/T | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
8 | 107388433 | intron variant | TAAATAAA/-;TAAA;TAAATAAATAAA | delins |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
8 | 107381731 | intron variant | A/G | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1.000 | 0.040 | 8 | 107263553 | intron variant | C/T | snv | 0.85 |
|
Eye Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
8 | 107281490 | intron variant | G/A | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
8 | 107328754 | intron variant | G/A;C | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
8 | 107339931 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
0.882 | 0.080 | 8 | 107366717 | intron variant | G/A | snv | 0.52 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.882 | 0.080 | 8 | 107366717 | intron variant | G/A | snv | 0.52 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.882 | 0.080 | 8 | 107366717 | intron variant | G/A | snv | 0.52 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.080 | 8 | 107250906 | 3 prime UTR variant | C/G | snv | 0.64 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.040 | 8 | 107250441 | 3 prime UTR variant | T/A | snv | 0.36 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
1.000 | 0.040 | 8 | 107250441 | 3 prime UTR variant | T/A | snv | 0.36 |
|
Female Urogenital Diseases and Pregnancy Complications | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.882 | 0.080 | 8 | 107330035 | intron variant | A/C;T | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.882 | 0.080 | 8 | 107330035 | intron variant | A/C;T | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.882 | 0.080 | 8 | 107330035 | intron variant | A/C;T | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.160 | 8 | 107347040 | missense variant | C/A | snv | 8.0E-06 | 1.4E-05 |
|
Behavior and Behavior Mechanisms | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
|
8 | 107422472 | intron variant | A/G | snv | 0.71 |
|
0.700 | 1.000 | 2 | 2018 | 2018 | ||||||||||
|
1.000 | 0.160 | 8 | 107347040 | missense variant | C/A | snv | 8.0E-06 | 1.4E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases | 0.020 | 1.000 | 2 | 2018 | 2019 |