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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 16 | 79211665 | stop gained | G/C;T | snv | 4.0E-06; 4.0E-06 |
|
0.800 | 1.000 | 2 | 2014 | 2014 | |||||||||
|
16 | 79315586 | regulatory region variant | T/C | snv | 0.59 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.925 | 16 | 79580219 | regulatory region variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
0.925 | 16 | 79580219 | regulatory region variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
0.925 | 16 | 79580219 | regulatory region variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
0.925 | 16 | 79580219 | regulatory region variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
0.925 | 16 | 79580219 | regulatory region variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
16 | 79415630 | intergenic variant | T/C | snv | 1.0E-02 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
16 | 79204666 | non coding transcript exon variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
16 | 79354312 | intergenic variant | G/A | snv | 0.47 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 16 | 79598995 | missense variant | T/G | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.040 | 16 | 79282918 | intergenic variant | A/G | snv | 0.74 |
|
Endocrine System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.882 | 0.080 | 16 | 79599040 | missense variant | C/G;T | snv | 4.1E-06 |
|
0.800 | 1.000 | 3 | 2002 | 2014 | ||||||||
|
1.000 | 0.080 | 16 | 79373021 | regulatory region variant | C/G;T | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.800 | 1.000 | 2 | 2011 | 2013 | ||||||||
|
0.882 | 0.080 | 16 | 79599040 | missense variant | C/G;T | snv | 4.1E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.882 | 0.080 | 16 | 79599040 | missense variant | C/G;T | snv | 4.1E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.882 | 0.080 | 16 | 79212426 | 3 prime UTR variant | G/A;C | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | < 0.001 | 1 | 2013 | 2013 | ||||||||
|
0.882 | 0.080 | 16 | 79212426 | 3 prime UTR variant | G/A;C | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | < 0.001 | 1 | 2013 | 2013 | ||||||||
|
0.882 | 0.080 | 16 | 79212426 | 3 prime UTR variant | G/A;C | snv |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | < 0.001 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.080 | 16 | 79211708 | stop gained | C/G;T | snv | 4.0E-06; 1.2E-05 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1.000 | 0.080 | 16 | 79211708 | stop gained | C/G;T | snv | 4.0E-06; 1.2E-05 |
|
Neoplasms; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1.000 | 0.080 | 16 | 79211708 | stop gained | C/G;T | snv | 4.0E-06; 1.2E-05 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.851 | 0.080 | 16 | 79516830 | downstream gene variant | C/A;T | snv |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.851 | 0.080 | 16 | 79516830 | downstream gene variant | C/A;T | snv |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.851 | 0.080 | 16 | 79516830 | downstream gene variant | C/A;T | snv |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 |