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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.658 | 0.600 | 11 | 102845217 | upstream gene variant | -/C;G | ins | 2.8E-04 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
11 | 102845217 | upstream gene variant | -/C;G | ins |
|
Pathological Conditions, Signs and Symptoms | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
0.851 | 0.040 | 11 | 102845217 | upstream gene variant | A/-;AA | delins |
|
Infections | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.851 | 0.040 | 11 | 102845217 | upstream gene variant | A/-;AA | delins |
|
Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.851 | 0.040 | 11 | 102845217 | upstream gene variant | A/-;AA | delins |
|
Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.851 | 0.040 | 11 | 102845217 | upstream gene variant | A/-;AA | delins |
|
Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.851 | 0.040 | 11 | 102845217 | upstream gene variant | A/-;AA | delins |
|
Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.040 | 11 | 102842734 | missense variant | A/C;G | snv | 4.0E-06; 0.57 |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.925 | 0.120 | 11 | 102838694 | synonymous variant | A/G | snv | 0.57 | 0.54 |
|
Nervous System Diseases; Mental Disorders | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||||
|
0.925 | 0.120 | 11 | 102838694 | synonymous variant | A/G | snv | 0.57 | 0.54 |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
11 | 102837183 | intron variant | A/G | snv | 0.54 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.040 | 11 | 102836635 | non coding transcript exon variant | A/T | snv | 0.10 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.040 | 11 | 102836635 | non coding transcript exon variant | A/T | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.040 | 11 | 102845095 | upstream gene variant | C/A | snv | 0.10 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.040 | 11 | 102845095 | upstream gene variant | C/A | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.882 | 0.120 | 11 | 102836608 | non coding transcript exon variant | C/A | snv | 0.54 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.882 | 0.120 | 11 | 102836608 | non coding transcript exon variant | C/A | snv | 0.54 |
|
Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.882 | 0.120 | 11 | 102836608 | non coding transcript exon variant | C/A | snv | 0.54 |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 11 | 102840850 | intron variant | C/G | snv | 0.11 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.040 | 11 | 102840850 | intron variant | C/G | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.040 | 11 | 102843480 | missense variant | C/T | snv | 4.0E-06 |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
11 | 102840709 | intron variant | C/T | snv | 2.1E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 102840709 | intron variant | C/T | snv | 2.1E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.080 | 11 | 102835973 | 3 prime UTR variant | C/T | snv | 2.0E-02 |
|
Nervous System Diseases; Mental Disorders | 0.010 | 1.000 | 1 | 2005 | 2005 | |||||||
|
1.000 | 0.040 | 11 | 102839740 | intron variant | C/T | snv | 0.10 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 |