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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
10 | 66465128 | intron variant | A/G | snv | 0.21 |
|
Respiratory Tract Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 10 | 67606868 | missense variant | A/T | snv |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
1.000 | 0.080 | 10 | 65983896 | intron variant | A/T | snv | 0.11 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.040 | 10 | 67085957 | intron variant | T/G | snv | 0.35 |
|
Nervous System Diseases | 0.720 | 0.667 | 3 | 2016 | 2018 | |||||||
|
1.000 | 0.040 | 10 | 66838534 | intron variant | C/A | snv | 0.29 |
|
Mental Disorders | 0.710 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1.000 | 0.040 | 10 | 66838534 | intron variant | C/A | snv | 0.29 |
|
Infections | 0.710 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1.000 | 0.040 | 10 | 66637687 | intron variant | A/G | snv | 0.67 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
10 | 66194307 | intron variant | T/C | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.080 | 10 | 67504839 | intron variant | G/C | snv | 0.13 |
|
Immune System Diseases; Nervous System Diseases | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
1.000 | 0.080 | 10 | 66001962 | intron variant | T/C | snv | 0.15 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.040 | 10 | 66919791 | intron variant | T/A | snv | 0.41 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.040 | 10 | 66919791 | intron variant | T/A | snv | 0.41 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.040 | 10 | 65948601 | intron variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
0.925 | 0.040 | 10 | 65948601 | intron variant | T/C;G | snv |
|
Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.040 | 10 | 67051026 | intron variant | G/A;C | snv |
|
Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.040 | 10 | 67051026 | intron variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
10 | 66417570 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
1.000 | 0.040 | 10 | 67192300 | intron variant | C/A | snv | 0.37 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2006 | 2006 | |||||||
|
10 | 67475334 | intron variant | T/C | snv | 1.4E-05 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
10 | 67453432 | intron variant | A/C;T | snv | 7.0E-06 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
10 | 67354852 | intron variant | G/A | snv | 5.6E-05 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 10 | 67151138 | intron variant | A/G | snv | 6.0E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.925 | 0.040 | 10 | 67413145 | intron variant | G/A;C;T | snv |
|
Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.040 | 10 | 67413145 | intron variant | G/A;C;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
0.925 | 0.080 | 10 | 65966714 | inframe deletion | CAA/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 0 |