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 | 14 | 79474040 | intron variant | G/T | snv | 0.21 |
|
0.800 | 1.000 | 2 | 2009 | 2015 | ||||||||
|
0.827 | 0.240 | 14 | 79478819 | intron variant | A/G | snv | 0.25 |
|
0.800 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
1.000 | 0.080 | 14 | 78319734 | intron variant | A/C | snv | 0.13 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.800 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.080 | 14 | 79437033 | intron variant | G/A | snv | 0.71 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.080 | 14 | 79433111 | intron variant | C/T | snv | 0.56 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.080 | 14 | 79433111 | intron variant | C/T | snv | 0.56 |
|
0.700 | 1.000 | 6 | 2015 | 2019 | ||||||||
|
14 | 79470621 | intron variant | T/C | snv | 0.26 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | ||||||||||
|
14 | 79470621 | intron variant | T/C | snv | 0.26 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | ||||||||||
|
14 | 79470621 | intron variant | T/C | snv | 0.26 |
|
0.700 | 1.000 | 2 | 2010 | 2019 | ||||||||||
|
14 | 78029418 | regulatory region variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 2 | 2019 | 2019 | ||||||||||
|
14 | 79473650 | intron variant | G/A | snv | 0.21 |
|
0.700 | 1.000 | 2 | 2015 | 2019 | ||||||||||
|
1.000 | 0.080 | 14 | 79474040 | intron variant | G/T | snv | 0.21 |
|
0.700 | 1.000 | 2 | 2018 | 2019 | ||||||||
|
14 | 79427703 | intron variant | G/A | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
14 | 79473182 | intron variant | C/T | snv | 0.25 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
0.827 | 0.240 | 14 | 79478819 | intron variant | A/G | snv | 0.25 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
14 | 79470621 | intron variant | T/C | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
1.000 | 0.040 | 14 | 78645876 | intron variant | C/T | snv | 0.11 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
14 | 79247254 | splice region variant | G/A | snv | 0.25 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
14 | 78825561 | intron variant | A/C | snv | 9.9E-02 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
14 | 79443776 | intron variant | C/T | snv | 0.21 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
14 | 79473650 | intron variant | G/A | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
14 | 79473650 | intron variant | G/A | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
1.000 | 0.080 | 14 | 78156180 | intergenic variant | A/G | snv | 0.18 |
|
Chemically-Induced Disorders; Mental Disorders | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
14 | 79105688 | intron variant | C/T | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
14 | 79424334 | intron variant | C/T | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2017 | 2017 |