OR5V1, olfactory receptor family 5 subfamily V member 1, 81696
N. diseases: 23; N. variants: 20
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
6 | 29404546 | intron variant | A/G;T | snv |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
6 | 29404546 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
1.000 | 0.120 | 6 | 29368277 | intron variant | G/A | snv | 0.59 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1.000 | 0.120 | 6 | 29373531 | 3 prime UTR variant | G/A | snv | 0.22 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
6 | 29355878 | missense variant | G/A;T | snv | 3.0E-02 | 7.1E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
6 | 29375578 | intron variant | C/T | snv | 0.20 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
0.790 | 0.320 | 6 | 29388554 | intron variant | A/G | snv | 5.8E-02 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.790 | 0.320 | 6 | 29388554 | intron variant | A/G | snv | 5.8E-02 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.790 | 0.320 | 6 | 29388554 | intron variant | A/G | snv | 5.8E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.790 | 0.320 | 6 | 29388554 | intron variant | A/G | snv | 5.8E-02 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.790 | 0.320 | 6 | 29388554 | intron variant | A/G | snv | 5.8E-02 |
|
Hemic and Lymphatic Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.790 | 0.320 | 6 | 29388554 | intron variant | A/G | snv | 5.8E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 6 | 29374540 | missense variant | A/G | snv | 1.2E-05 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.700 | 0 | ||||||||||
|
0.790 | 0.320 | 6 | 29388554 | intron variant | A/G | snv | 5.8E-02 |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.790 | 0.320 | 6 | 29388554 | intron variant | A/G | snv | 5.8E-02 |
|
Pathological Conditions, Signs and Symptoms | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.790 | 0.320 | 6 | 29388554 | intron variant | A/G | snv | 5.8E-02 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 |