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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.160 | 16 | 28862077 | intron variant | G/A | snv | 0.34 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.020 | 1.000 | 2 | 2011 | 2013 | |||||||
|
16 | 28859641 | intron variant | G/A | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
16 | 28859641 | intron variant | G/A | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
16 | 28859870 | intron variant | C/A;G | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
16 | 28852580 | intron variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
16 | 28851460 | intron variant | TTTTTTTT/-;TTTTTT;TTTTTTT;TTTTTTTTT;TTTTTTTTTTTTTTTTTT | delins | 0.34 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.925 | 0.120 | 16 | 28856483 | intron variant | C/T | snv | 0.34 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.120 | 16 | 28856483 | intron variant | C/T | snv | 0.34 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.851 | 0.160 | 16 | 28862077 | intron variant | G/A | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.851 | 0.160 | 16 | 28862077 | intron variant | G/A | snv | 0.34 |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.851 | 0.160 | 16 | 28862077 | intron variant | G/A | snv | 0.34 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.010 | < 0.001 | 1 | 2013 | 2013 | |||||||
|
0.851 | 0.160 | 16 | 28862077 | intron variant | G/A | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.851 | 0.160 | 16 | 28862077 | intron variant | G/A | snv | 0.34 |
|
Cardiovascular Diseases | 0.010 | < 0.001 | 1 | 2011 | 2011 | |||||||
|
16 | 28853150 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
16 | 28853721 | intron variant | T/C | snv | 0.34 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
16 | 28853721 | intron variant | T/C | snv | 0.34 |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
1.000 | 0.080 | 16 | 28860645 | intron variant | T/C | snv | 0.25 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.080 | 16 | 28860645 | intron variant | T/C | snv | 0.25 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
16 | 28869881 | intron variant | A/C | snv | 0.34 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
0.925 | 0.120 | 16 | 28871920 | missense variant | A/G;T | snv | 0.35 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.880 | 0.778 | 9 | 2011 | 2015 | |||||||
|
0.925 | 0.120 | 16 | 28871920 | missense variant | A/G;T | snv | 0.35 |
|
0.700 | 1.000 | 4 | 2009 | 2019 | ||||||||
|
0.925 | 0.120 | 16 | 28871920 | missense variant | A/G;T | snv | 0.35 |
|
0.700 | 1.000 | 2 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 16 | 28871920 | missense variant | A/G;T | snv | 0.35 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.020 | 1.000 | 2 | 2011 | 2014 | |||||||
|
0.925 | 0.120 | 16 | 28871920 | missense variant | A/G;T | snv | 0.35 |
|
0.700 | 1.000 | 2 | 2009 | 2009 | ||||||||
|
1.000 | 0.080 | 16 | 28866363 | missense variant | C/A | snv | 3.3E-04 | 1.2E-03 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 |