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 | 0.040 | 21 | 38447907 | intron variant | C/A;T | snv |
|
Cardiovascular Diseases | 0.720 | 1.000 | 3 | 2017 | 2020 | ||||||||
|
1.000 | 0.080 | 21 | 38466902 | intron variant | C/T | snv | 0.11 |
|
Immune System Diseases; Nervous System Diseases | 0.710 | 1.000 | 2 | 2016 | 2019 | |||||||
|
21 | 38611524 | intron variant | C/T | snv | 7.7E-03 |
|
0.700 | 1.000 | 2 | 2017 | 2019 | ||||||||||
|
21 | 38466112 | intron variant | T/A | snv | 0.46 |
|
0.700 | 1.000 | 2 | 2016 | 2019 | ||||||||||
|
21 | 38507058 | intron variant | G/C | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
21 | 38611524 | intron variant | C/T | snv | 7.7E-03 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
21 | 38606304 | intron variant | T/C | snv | 1.6E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1.000 | 0.080 | 21 | 38431740 | intron variant | T/C | snv | 0.27 |
|
Digestive System Diseases; Infections | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
21 | 38466112 | intron variant | T/A | snv | 0.46 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1.000 | 0.040 | 21 | 38493226 | intron variant | C/T | snv | 0.16 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
21 | 38498386 | 5 prime UTR variant | G/A | snv | 0.87 | 0.89 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
21 | 38465700 | intron variant | G/A | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
21 | 38433581 | intron variant | G/A | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
21 | 38482555 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
21 | 38482555 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
21 | 38480628 | intron variant | A/T | snv | 2.9E-02 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
21 | 38480628 | intron variant | A/T | snv | 2.9E-02 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
21 | 38473352 | intron variant | T/C | snv | 1.5E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
21 | 38479032 | intron variant | C/A | snv | 2.0E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.925 | 0.040 | 21 | 38635298 | intron variant | T/C;G | snv |
|
Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.040 | 21 | 38635298 | intron variant | T/C;G | snv |
|
Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
21 | 38493931 | intron variant | C/T | snv | 0.22 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
0.925 | 0.080 | 21 | 38403547 | missense variant | T/C | snv | 2.1E-05 |
|
Neoplasms; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.925 | 0.080 | 21 | 38403547 | missense variant | T/C | snv | 2.1E-05 |
|
Neoplasms; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1.000 | 0.040 | 21 | 38392384 | missense variant | T/C | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2010 | 2010 |