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 | 11860132 | upstream gene variant | C/A;T | snv |
|
0.700 | 1.000 | 2 | 2018 | 2018 | |||||||||||
|
0.776 | 0.240 | 1 | 11859214 | upstream gene variant | A/G | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1 | 11860132 | upstream gene variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
1 | 11860132 | upstream gene variant | C/A;T | snv |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.776 | 0.240 | 1 | 11859214 | upstream gene variant | A/G | snv | 0.39 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.040 | 0.750 | 4 | 2009 | 2015 | |||||||
|
0.851 | 0.160 | 1 | 11857283 | downstream gene variant | C/G;T | snv |
|
Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.851 | 0.160 | 1 | 11857283 | downstream gene variant | C/G;T | snv |
|
Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.851 | 0.160 | 1 | 11857283 | downstream gene variant | C/G;T | snv |
|
Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.851 | 0.160 | 1 | 11857283 | downstream gene variant | C/G;T | snv |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.776 | 0.240 | 1 | 11859214 | upstream gene variant | A/G | snv | 0.39 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 1 | 11859214 | upstream gene variant | A/G | snv | 0.39 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.776 | 0.240 | 1 | 11859214 | upstream gene variant | A/G | snv | 0.39 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.776 | 0.240 | 1 | 11859214 | upstream gene variant | A/G | snv | 0.39 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.776 | 0.240 | 1 | 11859214 | upstream gene variant | A/G | snv | 0.39 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 1 | 11859214 | upstream gene variant | A/G | snv | 0.39 |
|
Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.776 | 0.240 | 1 | 11859214 | upstream gene variant | A/G | snv | 0.39 |
|
Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.776 | 0.240 | 1 | 11859214 | upstream gene variant | A/G | snv | 0.39 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.925 | 0.160 | 1 | 11858427 | missense variant | C/T | snv | 5.0E-06 |
|
Nutritional and Metabolic Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.925 | 0.160 | 1 | 11858427 | missense variant | C/T | snv | 5.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 |