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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
7 | 95305887 | intron variant | A/- | delins |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
7 | 95311726 | intron variant | G/T | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 95308945 | intron variant | A/G | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
7 | 95308945 | intron variant | A/G | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 95320865 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||||
|
7 | 95316432 | intron variant | C/T | snv | 3.9E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 95313808 | intron variant | T/G | snv | 6.2E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 95310807 | intron variant | A/T | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 95308384 | intron variant | -/AA | delins | 0.42 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 95306923 | intron variant | A/C | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 95305887 | intron variant | A/- | delins | 0.30 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 95325307 | upstream gene variant | T/C | snv | 0.62 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
7 | 95325384 | upstream gene variant | C/G | snv | 0.40 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.040 | 7 | 95321453 | intron variant | C/T | snv | 3.7E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.040 | 7 | 95306310 | missense variant | G/C | snv | 4.0E-06 |
|
Eye Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
1.000 | 0.040 | 7 | 95311484 | missense variant | T/C | snv | 4.2E-04 | 1.0E-04 |
|
Eye Diseases | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
|
0.925 | 0.080 | 7 | 95298183 | 3 prime UTR variant | G/A | snv | 0.14 |
|
Cardiovascular Diseases | 0.020 | 1.000 | 2 | 2015 | 2018 | |||||||
|
1.000 | 0.080 | 7 | 95316748 | missense variant | C/T | snv |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
1.000 | 0.080 | 7 | 95316748 | missense variant | C/T | snv |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
1.000 | 0.080 | 7 | 95318487 | non coding transcript exon variant | G/A | snv | 0.26 |
|
Nutritional and Metabolic Diseases; Nervous System Diseases | 0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
0.925 | 0.080 | 7 | 95298183 | 3 prime UTR variant | G/A | snv | 0.14 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.925 | 0.080 | 7 | 95298183 | 3 prime UTR variant | G/A | snv | 0.14 |
|
Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.080 | 7 | 95324583 | upstream gene variant | G/A;C;T | snv |
|
Nervous System Diseases; Mental Disorders | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.080 | 7 | 95324583 | upstream gene variant | G/A;C;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.080 | 7 | 95324637 | upstream gene variant | T/C | snv | 0.72 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.010 | < 0.001 | 1 | 2013 | 2013 |