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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
3 | 49394470 | intron variant | C/T | snv | 0.19 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
3 | 49361826 | intron variant | G/A | snv | 0.28 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
3 | 49377358 | intron variant | C/T | snv | 0.30 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.040 | 3 | 49411133 | intron variant | A/C;T | snv |
|
Cardiovascular Diseases | 0.700 | 1.000 | 3 | 2017 | 2018 | ||||||||
|
1.000 | 0.040 | 3 | 49402292 | intron variant | A/T | snv | 0.24 |
|
Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1.000 | 0.040 | 3 | 49358927 | upstream gene variant | T/C | snv | 0.30 |
|
Musculoskeletal Diseases | 0.010 | < 0.001 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.040 | 3 | 49413431 | intron variant | A/G | snv | 0.40 |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2008 | 2008 | |||||||
|
1.000 | 0.040 | 3 | 49379392 | intron variant | G/A | snv | 0.29 |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
1.000 | 0.040 | 3 | 49363049 | intron variant | T/C | snv | 0.73 |
|
Eye Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.882 | 0.080 | 3 | 49375472 | missense variant | C/G;T | snv |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.080 | 3 | 49375472 | missense variant | C/G;T | snv |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.080 | 3 | 49375472 | missense variant | C/G;T | snv |
|
Neoplasms | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.080 | 3 | 49375472 | missense variant | C/G;T | snv |
|
Neoplasms | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.080 | 3 | 49360964 | missense variant | T/G | snv | 7.0E-06 |
|
Immune System Diseases; Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.080 | 3 | 49368647 | intron variant | T/C | snv | 0.43 |
|
Chemically-Induced Disorders; Mental Disorders | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.882 | 0.160 | 3 | 49375577 | missense variant | G/A | snv |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.160 | 3 | 49375577 | missense variant | G/A | snv |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.160 | 3 | 49375577 | missense variant | G/A | snv |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.160 | 3 | 49375577 | missense variant | G/A | snv |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.160 | 3 | 49375577 | missense variant | G/A | snv |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.160 | 3 | 49375465 | missense variant | T/A;C;G | snv |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.160 | 3 | 49375465 | missense variant | T/A;C;G | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.882 | 0.160 | 3 | 49375465 | missense variant | T/A;C;G | snv |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.160 | 3 | 49375465 | missense variant | T/A;C;G | snv |
|
Neoplasms | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.807 | 0.200 | 3 | 49375576 | missense variant | C/A;T | snv |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2016 | 2016 |