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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
7 | 92779056 | intron variant | C/T | snv | 0.14 |
|
0.800 | 1.000 | 7 | 2010 | 2019 | ||||||||||
|
7 | 92779056 | intron variant | C/T | snv | 0.14 |
|
0.800 | 1.000 | 4 | 2011 | 2019 | ||||||||||
|
1.000 | 0.120 | 7 | 92607515 | 3 prime UTR variant | A/G;T | snv |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.800 | 1.000 | 2 | 2014 | 2019 | ||||||||
|
1.000 | 7 | 92671484 | missense variant | C/T | snv | 7.0E-06 |
|
0.800 | 0 | ||||||||||||
|
7 | 92635096 | intron variant | T/C | snv | 0.38 |
|
0.700 | 1.000 | 3 | 2008 | 2009 | ||||||||||
|
7 | 92635096 | intron variant | T/C | snv | 0.38 |
|
0.700 | 1.000 | 3 | 2008 | 2009 | ||||||||||
|
7 | 92779056 | intron variant | C/T | snv | 0.14 |
|
0.700 | 1.000 | 3 | 2011 | 2018 | ||||||||||
|
7 | 92627591 | intron variant | C/T | snv | 0.64 |
|
0.700 | 1.000 | 2 | 2008 | 2009 | ||||||||||
|
1.000 | 0.080 | 7 | 92615108 | 3 prime UTR variant | C/T | snv | 0.19 | 0.19 |
|
0.700 | 1.000 | 2 | 2014 | 2019 | |||||||
|
7 | 92618762 | intron variant | C/T | snv | 0.32 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | ||||||||||
|
7 | 92618762 | intron variant | C/T | snv | 0.32 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | ||||||||||
|
7 | 92614358 | 3 prime UTR variant | G/A | snv | 0.28 |
|
0.700 | 1.000 | 2 | 2017 | 2019 | ||||||||||
|
7 | 92779056 | intron variant | C/T | snv | 0.14 |
|
0.700 | 1.000 | 2 | 2016 | 2018 | ||||||||||
|
7 | 92779056 | intron variant | C/T | snv | 0.14 |
|
0.700 | 1.000 | 2 | 2016 | 2018 | ||||||||||
|
0.882 | 0.080 | 7 | 92606850 | 3 prime UTR variant | T/A;C;G | snv |
|
0.700 | 1.000 | 2 | 2016 | 2019 | |||||||||
|
0.882 | 0.080 | 7 | 92606850 | 3 prime UTR variant | T/A;C;G | snv |
|
0.700 | 1.000 | 2 | 2016 | 2019 | |||||||||
|
7 | 92644264 | intron variant | C/T | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
7 | 92624658 | intron variant | G/A | snv | 0.36 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
7 | 92624658 | intron variant | G/A | snv | 0.36 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.080 | 7 | 92655809 | intron variant | A/G | snv | 0.36 |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
7 | 92627591 | intron variant | C/T | snv | 0.64 |
|
0.700 | 1.000 | 1 | 2008 | 2008 | ||||||||||
|
7 | 92627591 | intron variant | C/T | snv | 0.64 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 92635096 | intron variant | T/C | snv | 0.38 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
7 | 92635096 | intron variant | T/C | snv | 0.38 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
7 | 92635096 | intron variant | T/C | snv | 0.38 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 1.000 | 1 | 2019 | 2019 |