TRPM8, transient receptor potential cation channel subfamily M member 8, 79054
N. diseases: 127; N. variants: 9
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 233916724 | upstream gene variant | G/A | snv | 0.40 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
2 | 233916086 | upstream gene variant | A/G | snv | 0.40 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.925 | 0.040 | 2 | 233916448 | upstream gene variant | T/C | snv | 0.40 |
|
Nervous System Diseases | 0.870 | 1.000 | 10 | 2011 | 2019 | |||||||
|
0.925 | 0.040 | 2 | 233916448 | upstream gene variant | T/C | snv | 0.40 |
|
Nervous System Diseases | 0.710 | 1.000 | 2 | 2013 | 2019 | |||||||
|
0.925 | 0.040 | 2 | 233916448 | upstream gene variant | T/C | snv | 0.40 |
|
Nervous System Diseases | 0.020 | 1.000 | 2 | 2015 | 2019 | |||||||
|
0.925 | 0.040 | 2 | 233916448 | upstream gene variant | T/C | snv | 0.40 |
|
Pathological Conditions, Signs and Symptoms | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
2 | 233934849 | intron variant | C/T | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.120 | 2 | 233930302 | intron variant | G/C | snv | 0.11 |
|
Respiratory Tract Diseases; Immune System Diseases; Occupational Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
2 | 233919350 | intron variant | C/T | snv | 9.7E-02 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1.000 | 0.080 | 2 | 233945906 | synonymous variant | G/C | snv | 0.13 | 9.2E-02 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
|
0.925 | 0.040 | 2 | 233919016 | intron variant | G/A | snv | 7.8E-02 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.925 | 0.040 | 2 | 233919016 | intron variant | G/A | snv | 7.8E-02 |
|
Nervous System Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.925 | 0.040 | 2 | 233919016 | intron variant | G/A | snv | 7.8E-02 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.040 | 2 | 233944048 | intron variant | G/A | snv | 4.2E-02 |
|
Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 |