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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.807 | 0.120 | 15 | 58431740 | intron variant | G/A | snv | 0.33 |
|
0.800 | 1.000 | 7 | 2012 | 2019 | ||||||||
|
0.790 | 0.200 | 15 | 58431476 | intron variant | C/G;T | snv | 0.30 |
|
0.800 | 1.000 | 6 | 2012 | 2019 | ||||||||
|
0.790 | 0.200 | 15 | 58431476 | intron variant | C/G;T | snv | 0.30 |
|
0.800 | 1.000 | 5 | 2008 | 2019 | ||||||||
|
15 | 58434545 | intron variant | G/C | snv | 0.73 |
|
0.800 | 1.000 | 5 | 2010 | 2019 | ||||||||||
|
0.790 | 0.200 | 15 | 58431476 | intron variant | C/G;T | snv | 0.30 |
|
0.800 | 1.000 | 4 | 2012 | 2018 | ||||||||
|
15 | 58432593 | intron variant | T/A | snv | 0.33 |
|
0.800 | 1.000 | 4 | 2011 | 2019 | ||||||||||
|
15 | 58431227 | intron variant | A/G | snv | 0.34 |
|
0.800 | 1.000 | 3 | 2013 | 2019 | ||||||||||
|
0.851 | 0.120 | 15 | 58435126 | non coding transcript exon variant | A/G | snv | 0.80 |
|
0.800 | 1.000 | 3 | 2012 | 2018 | ||||||||
|
0.851 | 0.120 | 15 | 58435126 | non coding transcript exon variant | A/G | snv | 0.80 |
|
0.800 | 1.000 | 3 | 2012 | 2018 | ||||||||
|
15 | 58438954 | intron variant | G/A;C;T | snv |
|
0.800 | 1.000 | 3 | 2012 | 2019 | |||||||||||
|
15 | 58438954 | intron variant | G/A;C;T | snv |
|
0.800 | 1.000 | 3 | 2012 | 2019 | |||||||||||
|
0.807 | 0.120 | 15 | 58431740 | intron variant | G/A | snv | 0.33 |
|
0.800 | 1.000 | 2 | 2012 | 2017 | ||||||||
|
0.851 | 0.120 | 15 | 58435126 | non coding transcript exon variant | A/G | snv | 0.80 |
|
0.800 | 1.000 | 2 | 2012 | 2016 | ||||||||
|
15 | 58450219 | intron variant | G/A | snv | 0.81 |
|
0.800 | 1.000 | 2 | 2012 | 2018 | ||||||||||
|
15 | 58438954 | intron variant | G/A;C;T | snv |
|
0.800 | 1.000 | 2 | 2012 | 2018 | |||||||||||
|
15 | 58438299 | intron variant | C/G;T | snv |
|
0.800 | 1.000 | 2 | 2012 | 2017 | |||||||||||
|
15 | 58438299 | intron variant | C/G;T | snv |
|
0.800 | 1.000 | 2 | 2012 | 2013 | |||||||||||
|
1.000 | 0.040 | 15 | 58432325 | non coding transcript exon variant | A/G | snv | 0.38 |
|
0.800 | 1.000 | 2 | 2012 | 2017 | ||||||||
|
1.000 | 0.040 | 15 | 58563549 | missense variant | C/T | snv | 2.9E-03 | 2.9E-03 |
|
Nutritional and Metabolic Diseases | 0.800 | 0 | |||||||||
|
0.790 | 0.200 | 15 | 58431476 | intron variant | C/G;T | snv | 0.30 |
|
Cardiovascular Diseases | 0.720 | 1.000 | 3 | 2009 | 2013 | |||||||
|
0.925 | 0.080 | 15 | 58548387 | missense variant | C/T | snv | 1.0E-03 | 7.5E-04 |
|
Nutritional and Metabolic Diseases | 0.710 | 1.000 | 3 | 1991 | 1998 | ||||||
|
0.807 | 0.120 | 15 | 58431740 | intron variant | G/A | snv | 0.33 |
|
Eye Diseases | 0.710 | 1.000 | 2 | 2016 | 2019 | |||||||
|
0.807 | 0.120 | 15 | 58431740 | intron variant | G/A | snv | 0.33 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.710 | 1.000 | 1 | 2008 | 2008 | |||||||
|
15 | 58431280 | intron variant | T/C | snv | 0.34 |
|
0.700 | 1.000 | 5 | 2010 | 2019 | ||||||||||
|
15 | 58431227 | intron variant | A/G | snv | 0.34 |
|
0.700 | 1.000 | 5 | 2015 | 2019 |