ADIPOQ, adiponectin, C1Q and collagen domain containing, 9370
N. diseases: 679; N. variants: 45
Source: ALL
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.200 | 3 | 186852664 | non coding transcript exon variant | G/A | snv | 8.8E-02 |
|
0.800 | 1.000 | 2 | 2010 | 2017 | ||||||||
|
0.701 | 0.440 | 3 | 186842993 | intron variant | G/A | snv | 0.38 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 3 | 186855916 | 3 prime UTR variant | A/C;G | snv | 0.55 |
|
0.800 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 3 | 186854303 | missense variant | C/T | snv | 4.0E-06; 1.2E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases | 0.710 | 1.000 | 1 | 2003 | 2003 | |||||||
|
0.925 | 0.120 | 3 | 186854303 | missense variant | C/T | snv | 4.0E-06; 1.2E-05 |
|
0.700 | 1.000 | 1 | 2000 | 2000 | ||||||||
|
0.763 | 0.440 | 3 | 186853407 | intron variant | A/G | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
3 | 186841714 | upstream gene variant | G/T | snv |
|
0.700 | 0 | ||||||||||||||
|
0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.100 | 0.900 | 20 | 2002 | 2018 | |||||||
|
0.637 | 0.560 | 3 | 186841685 | upstream gene variant | C/A;G;T | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.100 | 1.000 | 14 | 2009 | 2019 | ||||||||
|
0.597 | 0.720 | 3 | 186853334 | intron variant | G/C;T | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.100 | 0.923 | 13 | 2009 | 2019 | ||||||||
|
0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 |
|
Cardiovascular Diseases | 0.100 | 0.923 | 13 | 2006 | 2019 | |||||||
|
0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.100 | 0.833 | 12 | 2004 | 2019 | |||||||
|
0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.100 | 0.727 | 11 | 2004 | 2019 | |||||||
|
0.597 | 0.720 | 3 | 186853334 | intron variant | G/C;T | snv |
|
Cardiovascular Diseases | 0.090 | 1.000 | 9 | 2012 | 2019 | ||||||||
|
0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 |
|
Digestive System Diseases; Neoplasms | 0.090 | 0.889 | 9 | 2013 | 2017 | |||||||
|
0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 |
|
Cardiovascular Diseases | 0.080 | 0.875 | 8 | 2005 | 2019 | |||||||
|
0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 |
|
Nutritional and Metabolic Diseases | 0.080 | 0.875 | 8 | 2011 | 2019 | |||||||
|
0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 |
|
Cardiovascular Diseases | 0.080 | 0.750 | 8 | 2006 | 2019 | |||||||
|
0.597 | 0.720 | 3 | 186853334 | intron variant | G/C;T | snv |
|
Cardiovascular Diseases | 0.070 | 1.000 | 7 | 2012 | 2018 | ||||||||
|
0.597 | 0.720 | 3 | 186853334 | intron variant | G/C;T | snv |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.060 | 1.000 | 6 | 2009 | 2019 | ||||||||
|
0.752 | 0.320 | 3 | 186841671 | upstream gene variant | G/A | snv | 5.3E-02 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.060 | 0.833 | 6 | 2011 | 2019 | |||||||
|
0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 |
|
Cardiovascular Diseases | 0.060 | 1.000 | 6 | 2010 | 2018 | |||||||
|
0.637 | 0.560 | 3 | 186841685 | upstream gene variant | C/A;G;T | snv |
|
Digestive System Diseases; Neoplasms | 0.060 | 0.833 | 6 | 2008 | 2017 | ||||||||
|
0.637 | 0.560 | 3 | 186841685 | upstream gene variant | C/A;G;T | snv |
|
Nutritional and Metabolic Diseases | 0.060 | 1.000 | 6 | 2010 | 2017 | ||||||||
|
0.637 | 0.560 | 3 | 186841685 | upstream gene variant | C/A;G;T | snv |
|
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.060 | 1.000 | 6 | 2010 | 2019 |