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 | 10 | 67905124 | intron variant | T/C;G | snv |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.742 | 0.480 | 10 | 67883584 | upstream gene variant | T/C | snv | 0.64 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.030 | 0.667 | 3 | 2010 | 2020 | |||||||
|
0.925 | 0.080 | 10 | 67891367 | intron variant | A/G;T | snv | 0.52; 8.0E-06 | 0.47 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.030 | 1.000 | 3 | 2011 | 2020 | ||||||
|
0.925 | 0.160 | 10 | 67900736 | intron variant | G/A | snv | 7.1E-02 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases | 0.020 | 1.000 | 2 | 2017 | 2018 | |||||||
|
0.724 | 0.480 | 10 | 67883321 | upstream gene variant | T/C;G | snv |
|
Neoplasms; Nervous System Diseases; Endocrine System Diseases | 0.020 | 1.000 | 2 | 2017 | 2019 | ||||||||
|
0.724 | 0.480 | 10 | 67883321 | upstream gene variant | T/C;G | snv |
|
Eye Diseases | 0.020 | 1.000 | 2 | 2015 | 2019 | ||||||||
|
0.776 | 0.320 | 10 | 67915401 | intron variant | A/G | snv | 0.46 |
|
Cardiovascular Diseases | 0.020 | 1.000 | 2 | 2017 | 2018 | |||||||
|
0.790 | 0.360 | 10 | 67906841 | synonymous variant | T/C | snv | 0.11 | 7.1E-02 |
|
Cardiovascular Diseases | 0.020 | 1.000 | 2 | 2011 | 2015 | ||||||
|
0.790 | 0.440 | 10 | 67903362 | intron variant | C/G | snv | 0.64 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.020 | 1.000 | 2 | 2008 | 2011 | |||||||
|
0.925 | 0.160 | 10 | 67900736 | intron variant | G/A | snv | 7.1E-02 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 10 | 67908257 | intron variant | G/T | snv | 0.47 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1.000 | 0.040 | 10 | 67908257 | intron variant | G/T | snv | 0.47 |
|
Behavior and Behavior Mechanisms | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.925 | 0.080 | 10 | 67913178 | intron variant | T/C | snv | 4.1E-03 |
|
Behavior and Behavior Mechanisms | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.080 | 10 | 67913178 | intron variant | T/C | snv | 4.1E-03 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.080 | 10 | 67913178 | intron variant | T/C | snv | 4.1E-03 |
|
Behavior and Behavior Mechanisms | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.080 | 10 | 67894017 | intron variant | A/G | snv | 0.11 |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.925 | 0.080 | 10 | 67894017 | intron variant | A/G | snv | 0.11 |
|
Digestive System Diseases; Chemically-Induced Disorders | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.040 | 10 | 67892108 | intron variant | G/A | snv | 0.11 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.724 | 0.480 | 10 | 67883321 | upstream gene variant | T/C;G | snv |
|
Skin and Connective Tissue Diseases; Immune System Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.724 | 0.480 | 10 | 67883321 | upstream gene variant | T/C;G | snv |
|
Skin and Connective Tissue Diseases; Endocrine System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.724 | 0.480 | 10 | 67883321 | upstream gene variant | T/C;G | snv |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.724 | 0.480 | 10 | 67883321 | upstream gene variant | T/C;G | snv |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.724 | 0.480 | 10 | 67883321 | upstream gene variant | T/C;G | snv |
|
Nervous System Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.724 | 0.480 | 10 | 67883321 | upstream gene variant | T/C;G | snv |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.724 | 0.480 | 10 | 67883321 | upstream gene variant | T/C;G | snv |
|
Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 |