HSPA1B, heat shock protein family A (Hsp70) member 1B, 3304
N. diseases: 251; N. variants: 4
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.080 | 6 | 31828202 | missense variant | G/A;T | snv | 1.9E-05 |
|
0.010 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.827 | 0.360 | 6 | 31826815 | upstream gene variant | C/T | snv | 0.45 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.851 | 0.200 | 6 | 31827773 | 5 prime UTR variant | C/G;T | snv | 8.5E-05; 9.3E-02; 1.4E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.080 | 6 | 31828202 | missense variant | G/A;T | snv | 1.9E-05 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.925 | 0.080 | 6 | 31829810 | synonymous variant | C/G | snv | 0.57 | 0.52 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2020 | 2020 | ||||||
|
0.827 | 0.360 | 6 | 31826815 | upstream gene variant | C/T | snv | 0.45 |
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.827 | 0.360 | 6 | 31826815 | upstream gene variant | C/T | snv | 0.45 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.851 | 0.200 | 6 | 31827773 | 5 prime UTR variant | C/G;T | snv | 8.5E-05; 9.3E-02; 1.4E-05 |
|
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.080 | 6 | 31829810 | synonymous variant | C/G | snv | 0.57 | 0.52 |
|
Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
|
0.827 | 0.360 | 6 | 31826815 | upstream gene variant | C/T | snv | 0.45 |
|
Respiratory Tract Diseases | 0.700 | 0 | ||||||||||
|
0.851 | 0.200 | 6 | 31827773 | 5 prime UTR variant | C/G;T | snv | 8.5E-05; 9.3E-02; 1.4E-05 |
|
Respiratory Tract Diseases | 0.700 | 0 | ||||||||||
|
0.851 | 0.200 | 6 | 31827773 | 5 prime UTR variant | C/G;T | snv | 8.5E-05; 9.3E-02; 1.4E-05 |
|
Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.827 | 0.360 | 6 | 31826815 | upstream gene variant | C/T | snv | 0.45 |
|
Skin and Connective Tissue Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 |