MEF2D, myocyte enhancer factor 2D, 4209
N. diseases: 72; 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.040 | 1 | 156476450 | intron variant | C/A | snv | 0.62 | 0.54 |
|
Nervous System Diseases | 0.820 | 0.500 | 4 | 2012 | 2017 | ||||||
|
1 | 156480948 | missense variant | G/A;C | snv | 0.62 |
|
Nervous System Diseases | 0.800 | 1.000 | 2 | 2012 | 2016 | |||||||||
|
1 | 156486509 | intron variant | C/T | snv | 0.54 |
|
Nervous System Diseases | 0.800 | 1.000 | 2 | 2012 | 2013 | |||||||||
|
1 | 156486509 | intron variant | -/T | delins |
|
Nervous System Diseases | 0.700 | 1.000 | 2 | 2012 | 2013 | ||||||||||
|
1 | 156464911 | 3 prime UTR variant | G/T | snv | 0.54 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1 | 156481081 | intron variant | T/C | snv | 0.62 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
1 | 156491915 | intron variant | A/T | snv | 0.54 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 |