rs1557137745
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Using a large international sample to investigate epilepsy in Rett syndrome.
|
23421866 |
2013 |
rs28934906
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Using a large international sample to investigate epilepsy in Rett syndrome.
|
23421866 |
2013 |
rs61748396
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Using a large international sample to investigate epilepsy in Rett syndrome.
|
23421866 |
2013 |
rs61749724
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Using a large international sample to investigate epilepsy in Rett syndrome.
|
23421866 |
2013 |
rs61750240
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Using a large international sample to investigate epilepsy in Rett syndrome.
|
23421866 |
2013 |
rs61750241
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Using a large international sample to investigate epilepsy in Rett syndrome.
|
23421866 |
2013 |
rs61751443
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Using a large international sample to investigate epilepsy in Rett syndrome.
|
23421866 |
2013 |
rs1557136758
|
|
CT |
0.700 |
CausalMutation |
CLINVAR |
Rett syndrome: revised diagnostic criteria and nomenclature.
|
21154482 |
2010 |
rs1557137745
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Rett syndrome: revised diagnostic criteria and nomenclature.
|
21154482 |
2010 |
rs28934906
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Rett syndrome: revised diagnostic criteria and nomenclature.
|
21154482 |
2010 |
rs61748396
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Rett syndrome: revised diagnostic criteria and nomenclature.
|
21154482 |
2010 |
rs61749724
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Rett syndrome: revised diagnostic criteria and nomenclature.
|
21154482 |
2010 |
rs61750240
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Rett syndrome: revised diagnostic criteria and nomenclature.
|
21154482 |
2010 |
rs61750241
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Rett syndrome: revised diagnostic criteria and nomenclature.
|
21154482 |
2010 |
rs61751443
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Rett syndrome: revised diagnostic criteria and nomenclature.
|
21154482 |
2010 |
rs1557136758
|
|
CT |
0.700 |
CausalMutation |
CLINVAR |
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
|
18337588 |
2008 |
rs1557137745
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
|
18337588 |
2008 |
rs28934906
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
|
18337588 |
2008 |
rs61748396
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
|
18337588 |
2008 |
rs61749724
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
|
18337588 |
2008 |
rs61750240
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
|
18337588 |
2008 |
rs61750241
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
|
18337588 |
2008 |
rs61751443
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
|
18337588 |
2008 |
rs1557136758
|
|
CT |
0.700 |
CausalMutation |
CLINVAR |
MECP2 mutations in males.
|
17351020 |
2007 |
rs1557136758
|
|
CT |
0.700 |
CausalMutation |
CLINVAR |
Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.
|
17267601 |
2007 |