STAT4, signal transducer and activator of transcription 4, 6775
N. diseases: 13; N. variants: 17
Source: GWASDB ×
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 |
|
Skin and Connective Tissue Diseases; Immune System Diseases | 0.900 | 0.967 | 7 | 2007 | 2017 | |||||||
|
0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.900 | 0.966 | 3 | 2007 | 2017 | |||||||
|
0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 |
|
Digestive System Diseases; Neoplasms | 0.900 | 0.909 | 1 | 2013 | 2019 | |||||||
|
0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 |
|
Immune System Diseases | 0.900 | 1.000 | 1 | 2008 | 2017 | |||||||
|
0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 |
|
Skin and Connective Tissue Diseases | 0.870 | 0.778 | 1 | 2009 | 2017 | |||||||
|
0.763 | 0.360 | 2 | 191105153 | intron variant | G/C | snv | 0.79 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.820 | 1.000 | 1 | 2012 | 2017 | |||||||
|
0.882 | 0.160 | 2 | 191038032 | intron variant | G/A | snv | 0.25 |
|
Skin and Connective Tissue Diseases; Immune System Diseases | 0.810 | 1.000 | 2 | 2008 | 2016 | |||||||
|
1.000 | 0.200 | 2 | 191145762 | intron variant | A/C | snv | 0.55 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases | 0.810 | 1.000 | 2 | 2012 | 2015 | |||||||
|
0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.810 | 1.000 | 1 | 2012 | 2014 | |||||||
|
0.882 | 0.160 | 2 | 191075725 | intron variant | G/A;T | snv |
|
Skin and Connective Tissue Diseases; Immune System Diseases | 0.810 | 1.000 | 1 | 2010 | 2013 | ||||||||
|
0.925 | 0.120 | 2 | 191078546 | intron variant | A/T | snv | 3.6E-02 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.800 | 1.000 | 2 | 2012 | 2012 | |||||||
|
0.882 | 0.160 | 2 | 191038032 | intron variant | G/A | snv | 0.25 |
|
Skin and Connective Tissue Diseases | 0.800 | 1.000 | 2 | 2010 | 2019 | |||||||
|
1.000 | 0.080 | 2 | 191048308 | intron variant | A/G | snv | 6.1E-02 |
|
Digestive System Diseases; Nutritional and Metabolic Diseases | 0.800 | 1.000 | 2 | 2011 | 2012 | |||||||
|
0.776 | 0.400 | 2 | 191071078 | intron variant | C/T | snv | 0.19 |
|
Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.724 | 0.200 | 2 | 191108308 | intron variant | G/A | snv | 0.70 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.732 | 0.480 | 2 | 191079016 | intron variant | C/T | snv | 0.21 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.800 | 1.000 | 1 | 2014 | 2019 | |||||||
|
0.925 | 0.200 | 2 | 191068528 | 3 prime UTR variant | G/A | snv | 0.20 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.800 | 1.000 | 1 | 2012 | 2015 | |||||||
|
0.851 | 0.160 | 2 | 191066738 | intron variant | A/C | snv | 0.45 |
|
Digestive System Diseases | 0.800 | 1.000 | 1 | 2012 | 2015 | |||||||
|
1.000 | 0.200 | 2 | 191150346 | intron variant | A/C;G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases | 0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 |
|
Immune System Diseases | 0.800 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.882 | 0.160 | 2 | 191075725 | intron variant | G/A;T | snv |
|
Skin and Connective Tissue Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.851 | 0.280 | 2 | 191153045 | upstream gene variant | T/C | snv | 0.54 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases | 0.800 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.776 | 0.400 | 2 | 191071078 | intron variant | C/T | snv | 0.19 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 2 | 2012 | 2012 | |||||||
|
0.776 | 0.400 | 2 | 191071078 | intron variant | C/T | snv | 0.19 |
|
Skin and Connective Tissue Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.827 | 0.240 | 2 | 191090126 | intron variant | G/A | snv | 0.66 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2013 | 2013 |