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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.080 | 10 | 52764898 | downstream gene variant | G/A | snv | 0.29 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.080 | 10 | 52764898 | downstream gene variant | G/A | snv | 0.29 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
10 | 52766446 | 3 prime UTR variant | C/T | snv | 0.48 |
|
Infections | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.827 | 0.200 | 10 | 52771774 | upstream gene variant | G/A | snv | 0.30 |
|
Digestive System Diseases; Infections | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.827 | 0.200 | 10 | 52771774 | upstream gene variant | G/A | snv | 0.30 |
|
Pathological Conditions, Signs and Symptoms | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.827 | 0.200 | 10 | 52771774 | upstream gene variant | G/A | snv | 0.30 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.827 | 0.200 | 10 | 52771774 | upstream gene variant | G/A | snv | 0.30 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.827 | 0.200 | 10 | 52771774 | upstream gene variant | G/A | snv | 0.30 |
|
Infections | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.827 | 0.200 | 10 | 52771774 | upstream gene variant | G/A | snv | 0.30 |
|
Female Urogenital Diseases and Pregnancy Complications; Infections | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.040 | 10 | 52772131 | upstream gene variant | T/G | snv | 0.30 |
|
Infections | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.040 | 10 | 52772131 | upstream gene variant | T/G | snv | 0.30 |
|
Infections | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.790 | 0.480 | 10 | 52772254 | upstream gene variant | G/C | snv | 0.31 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.790 | 0.480 | 10 | 52772254 | upstream gene variant | G/C | snv | 0.31 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2020 | 2020 | |||||||
|
0.790 | 0.480 | 10 | 52772254 | upstream gene variant | G/C | snv | 0.31 |
|
Infections; Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.080 | 10 | 52771481 | missense variant | C/T | snv | 6.4E-05 | 4.9E-05 |
|
Skin and Connective Tissue Diseases; Immune System Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
|
0.662 | 0.640 | 10 | 52771475 | missense variant | C/T | snv | 0.14 | 0.11 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2020 | 2020 | ||||||
|
0.662 | 0.640 | 10 | 52771475 | missense variant | C/T | snv | 0.14 | 0.11 |
|
Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.662 | 0.640 | 10 | 52771475 | missense variant | C/T | snv | 0.14 | 0.11 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
0.662 | 0.640 | 10 | 52771475 | missense variant | C/T | snv | 0.14 | 0.11 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.662 | 0.640 | 10 | 52771475 | missense variant | C/T | snv | 0.14 | 0.11 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
|
0.662 | 0.640 | 10 | 52771475 | missense variant | C/T | snv | 0.14 | 0.11 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
0.662 | 0.640 | 10 | 52771475 | missense variant | C/T | snv | 0.14 | 0.11 |
|
Infections; Immune System Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.662 | 0.640 | 10 | 52771475 | missense variant | C/T | snv | 0.14 | 0.11 |
|
Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
|
0.662 | 0.640 | 10 | 52771475 | missense variant | C/T | snv | 0.14 | 0.11 |
|
Pathological Conditions, Signs and Symptoms | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
0.662 | 0.640 | 10 | 52771475 | missense variant | C/T | snv | 0.14 | 0.11 |
|
Infections | 0.010 | 1.000 | 1 | 2010 | 2010 |