MRVI1, murine retrovirus integration site 1 homolog, 10335
N. diseases: 20; 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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
11 | 10652497 | intron variant | C/G | snv | 0.78 |
|
Nervous System Diseases | 0.700 | 1.000 | 2 | 2016 | 2016 | |||||||||
|
11 | 10643688 | intron variant | C/T | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
11 | 10597494 | intron variant | T/A | snv | 4.4E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.925 | 0.080 | 11 | 10642486 | intron variant | G/T | snv | 0.22 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.080 | 11 | 10642486 | intron variant | G/T | snv | 0.22 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.160 | 11 | 10628820 | missense variant | G/A | snv | 5.6E-02 | 5.0E-02 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
|
0.925 | 0.160 | 11 | 10628820 | missense variant | G/A | snv | 5.6E-02 | 5.0E-02 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
|
11 | 10652192 | missense variant | T/A;C | snv | 0.76 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
11 | 10652192 | missense variant | T/A;C | snv | 0.76 |
|
Nervous System Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
11 | 10652497 | intron variant | C/G | snv | 0.78 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
11 | 10645728 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
11 | 10686942 | intron variant | C/G | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1.000 | 0.080 | 11 | 10639293 | intron variant | G/T | snv | 0.24 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
11 | 10647681 | intron variant | T/A;C;G | snv |
|
0.700 | 1.000 | 1 | 2010 | 2010 |