CYP2C8, cytochrome P450 family 2 subfamily C member 8, 1558
N. diseases: 73; N. variants: 14
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.807 | 0.160 | 10 | 95038992 | missense variant | T/C | snv | 8.3E-02 | 8.0E-02 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
|
0.882 | 0.160 | 10 | 95067273 | missense variant | C/A;T | snv | 8.3E-02 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.925 | 0.160 | 10 | 95038791 | intron variant | C/T | snv | 0.24 |
|
Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.120 | 10 | 95042841 | intron variant | A/C;T | snv | 0.58 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.160 | 10 | 95038791 | intron variant | C/T | snv | 0.24 |
|
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2008 | 2008 | |||||||
|
0.925 | 0.080 | 10 | 95069772 | upstream gene variant | A/C | snv | 0.11 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.807 | 0.160 | 10 | 95038992 | missense variant | T/C | snv | 8.3E-02 | 8.0E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
|
0.882 | 0.040 | 10 | 95058362 | missense variant | G/A;C | snv | 1.0E-04; 3.7E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.851 | 0.120 | 10 | 95058349 | missense variant | T/A | snv | 1.6E-02 | 4.9E-02 |
|
Cardiovascular Diseases | 0.010 | < 0.001 | 1 | 2007 | 2007 | ||||||
|
0.882 | 0.040 | 10 | 95069271 | missense variant | C/A | snv | 4.0E-06 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.807 | 0.160 | 10 | 95038992 | missense variant | T/C | snv | 8.3E-02 | 8.0E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
|
0.882 | 0.040 | 10 | 95058362 | missense variant | G/A;C | snv | 1.0E-04; 3.7E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.851 | 0.120 | 10 | 95058349 | missense variant | T/A | snv | 1.6E-02 | 4.9E-02 |
|
Cardiovascular Diseases | 0.010 | < 0.001 | 1 | 2007 | 2007 | ||||||
|
0.882 | 0.040 | 10 | 95069271 | missense variant | C/A | snv | 4.0E-06 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.807 | 0.160 | 10 | 95038992 | missense variant | T/C | snv | 8.3E-02 | 8.0E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
|
0.882 | 0.040 | 10 | 95058362 | missense variant | G/A;C | snv | 1.0E-04; 3.7E-02 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.851 | 0.120 | 10 | 95058349 | missense variant | T/A | snv | 1.6E-02 | 4.9E-02 |
|
Cardiovascular Diseases | 0.010 | < 0.001 | 1 | 2007 | 2007 | ||||||
|
0.882 | 0.040 | 10 | 95069271 | missense variant | C/A | snv | 4.0E-06 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
1.000 | 0.040 | 10 | 95037713 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.882 | 0.160 | 10 | 95067273 | missense variant | C/A;T | snv | 8.3E-02 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.851 | 0.120 | 10 | 95058349 | missense variant | T/A | snv | 1.6E-02 | 4.9E-02 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1.000 | 0.080 | 10 | 95067259 | missense variant | G/A;C | snv | 1.6E-05; 7.2E-04 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 10 | 95067214 | frameshift variant | T/- | delins | 1.5E-04 | 4.2E-05 |
|
0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 10 | 95037713 | intron variant | C/A;T | snv |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 10 | 95069673 | upstream gene variant | G/T | snv | 0.18 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 |