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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
19 | 10277786 | intron variant | G/A | snv | 2.1E-03 |
|
0.700 | 1.000 | 2 | 2012 | 2012 | ||||||||||
|
19 | 10277786 | intron variant | G/A | snv | 2.1E-03 |
|
0.700 | 1.000 | 2 | 2012 | 2012 | ||||||||||
|
19 | 10284797 | missense variant | G/A | snv |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||||
|
19 | 10281703 | intron variant | -/C | delins | 7.6E-04 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
19 | 10269461 | intron variant | G/A | snv | 3.4E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
19 | 10269461 | intron variant | G/A | snv | 3.4E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
19 | 10269461 | intron variant | G/A | snv | 3.4E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
19 | 10269461 | intron variant | G/A | snv | 3.4E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
19 | 10269461 | intron variant | G/A | snv | 3.4E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
19 | 10277786 | intron variant | G/A | snv | 2.1E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
19 | 10278833 | intron variant | C/T | snv | 6.8E-04 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
19 | 10278833 | intron variant | C/T | snv | 6.8E-04 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
19 | 10278833 | intron variant | C/T | snv | 6.8E-04 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
19 | 10278833 | intron variant | C/T | snv | 6.8E-04 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
19 | 10286167 | 3 prime UTR variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
19 | 10281711 | intron variant | G/A;C;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
19 | 10286554 | 3 prime UTR variant | C/T | snv | 3.1E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.090 | 0.778 | 9 | 2005 | 2019 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Cardiovascular Diseases | 0.090 | 1.000 | 9 | 2009 | 2019 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Cardiovascular Diseases | 0.060 | 0.833 | 6 | 2004 | 2018 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Digestive System Diseases | 0.060 | 1.000 | 6 | 2003 | 2015 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases | 0.060 | 0.500 | 6 | 2006 | 2018 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Cardiovascular Diseases | 0.060 | 1.000 | 6 | 2009 | 2018 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases | 0.050 | 1.000 | 5 | 2006 | 2018 | ||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.050 | 1.000 | 5 | 2003 | 2019 |