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 | 64214130 | intron variant | A/C;G;T | snv |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.800 | 1.000 | 2 | 2012 | 2017 | ||||||||
|
1.000 | 14 | 64210033 | missense variant | C/G;T | snv | 4.0E-06; 4.8E-03 |
|
0.800 | 1.000 | 1 | 2007 | 2007 | |||||||||
|
0.925 | 0.080 | 14 | 64227194 | 3 prime UTR variant | C/T | snv | 2.4E-02 |
|
Neoplasms; Male Urogenital Diseases | 0.710 | 1.000 | 1 | 2015 | 2015 | |||||||
|
14 | 64236875 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 2 | 2016 | 2019 | |||||||||||
|
1.000 | 0.080 | 14 | 64213242 | intron variant | A/G | snv | 0.63 |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.700 | 1.000 | 2 | 2018 | 2018 | |||||||
|
14 | 64245143 | intron variant | A/G | snv | 4.4E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.040 | 14 | 64230319 | intron variant | T/A;C | snv |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
14 | 64244659 | intron variant | C/T | snv | 4.4E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
14 | 64244659 | intron variant | C/T | snv | 4.4E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.925 | 0.200 | 14 | 64256807 | intron variant | G/A | snv | 0.41 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.827 | 0.240 | 14 | 64280452 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.790 | 0.200 | 14 | 64279461 | intron variant | G/A;T | snv | 0.57 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
14 | 64278681 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
14 | 64236875 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
14 | 64236875 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
14 | 64236875 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
14 | 64160241 | intron variant | C/T | snv | 1.6E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
14 | 64226667 | intron variant | G/A | snv | 0.25 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 14 | 64093374 | stop gained | G/A | snv | 8.5E-02 | 8.9E-02 |
|
Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
1.000 | 0.080 | 14 | 64253546 | intron variant | T/C | snv | 0.41 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 14 | 64259785 | intron variant | A/G | snv | 0.41 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.040 | 14 | 64259785 | intron variant | A/G | snv | 0.41 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.040 | 14 | 64219489 | intron variant | A/G;T | snv |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 14 | 64107608 | splice donor variant | G/A;T | snv | 4.0E-06 | 7.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.645 | 0.560 | 14 | 64257333 | synonymous variant | C/T | snv | 6.7E-02 | 6.3E-02 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.040 | 0.500 | 4 | 2005 | 2018 |