TRPA1, transient receptor potential cation channel subfamily A member 1, 8989
N. diseases: 160; N. variants: 10
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
8 | 72096014 | intron variant | C/A;T | snv | 8.2E-02 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.882 | 0.040 | 8 | 72034369 | missense variant | T/C | snv |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
8 | 72037366 | intron variant | C/G;T | snv |
|
Pathological Conditions, Signs and Symptoms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||||
|
1.000 | 0.080 | 8 | 72024002 | intron variant | C/A | snv | 0.48 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
8 | 72036453 | missense variant | C/A;G | snv | 1.6E-05 |
|
Pathological Conditions, Signs and Symptoms | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
1.000 | 0.080 | 8 | 72062571 | intron variant | C/T | snv | 0.16 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.882 | 0.040 | 8 | 72034369 | missense variant | T/C | snv |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.882 | 0.040 | 8 | 72034369 | missense variant | T/C | snv |
|
0.010 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
1.000 | 0.080 | 8 | 72028626 | intron variant | A/G | snv | 0.68 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.080 | 8 | 72070130 | intron variant | A/C | snv | 0.69 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.925 | 0.160 | 8 | 72065468 | missense variant | C/T | snv | 0.14 | 0.16 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
0.925 | 0.160 | 8 | 72065468 | missense variant | C/T | snv | 0.14 | 0.16 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.925 | 0.160 | 8 | 72065468 | missense variant | C/T | snv | 0.14 | 0.16 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1.000 | 0.080 | 8 | 72023604 | intron variant | G/T | snv | 0.48 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 |