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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
15 | 58452149 | intron variant | T/G | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
15 | 58459002 | intron variant | T/A | snv | 7.6E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
15 | 58507555 | intron variant | A/G | snv | 2.2E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
15 | 58507555 | intron variant | A/G | snv | 2.2E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
15 | 58507555 | intron variant | A/G | snv | 2.2E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
15 | 58520578 | intron variant | C/T | snv | 5.4E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
15 | 58431280 | intron variant | T/C | snv | 0.34 |
|
0.700 | 1.000 | 5 | 2010 | 2019 | ||||||||||
|
15 | 58431280 | intron variant | T/C | snv | 0.34 |
|
0.700 | 1.000 | 2 | 2018 | 2019 | ||||||||||
|
15 | 58431280 | intron variant | T/C | snv | 0.34 |
|
0.700 | 1.000 | 2 | 2017 | 2018 | ||||||||||
|
15 | 58431280 | intron variant | T/C | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
15 | 58431280 | intron variant | T/C | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
15 | 58431227 | intron variant | A/G | snv | 0.34 |
|
0.700 | 1.000 | 5 | 2015 | 2019 | ||||||||||
|
15 | 58431227 | intron variant | A/G | snv | 0.34 |
|
0.800 | 1.000 | 3 | 2013 | 2019 | ||||||||||
|
15 | 58431227 | intron variant | A/G | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
15 | 58431227 | intron variant | A/G | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
15 | 58431227 | intron variant | A/G | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
15 | 58418428 | intron variant | C/A | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
15 | 58429415 | intron variant | G/A | snv | 0.36 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.040 | 15 | 58563549 | missense variant | C/T | snv | 2.9E-03 | 2.9E-03 |
|
Nutritional and Metabolic Diseases | 0.800 | 0 | |||||||||
|
1.000 | 0.040 | 15 | 58432184 | non coding transcript exon variant | A/G | snv | 5.6E-02 |
|
Nutritional and Metabolic Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
15 | 58432507 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
15 | 58432507 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
15 | 58432507 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
15 | 58545523 | intron variant | G/A | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
15 | 58427542 | intron variant | G/A | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2012 | 2012 |