rs1557136758
|
|
CT |
0.700 |
CausalMutation |
CLINVAR |
Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study.
|
27354166 |
2016 |
rs1557137745
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study.
|
27354166 |
2016 |
rs28934906
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study.
|
27354166 |
2016 |
rs61748396
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study.
|
27354166 |
2016 |
rs61749724
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study.
|
27354166 |
2016 |
rs61750240
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study.
|
27354166 |
2016 |
rs61750241
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study.
|
27354166 |
2016 |
rs61751443
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study.
|
27354166 |
2016 |
rs1557136758
|
|
CT |
0.700 |
CausalMutation |
CLINVAR |
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
|
24399845 |
2014 |
rs1557136758
|
|
CT |
0.700 |
CausalMutation |
CLINVAR |
MECP2 duplication: possible cause of severe phenotype in females.
|
24458799 |
2014 |
rs1557137745
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
MECP2 duplication: possible cause of severe phenotype in females.
|
24458799 |
2014 |
rs1557137745
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
|
24399845 |
2014 |
rs28934906
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
MECP2 duplication: possible cause of severe phenotype in females.
|
24458799 |
2014 |
rs28934906
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
|
24399845 |
2014 |
rs61748396
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
MECP2 duplication: possible cause of severe phenotype in females.
|
24458799 |
2014 |
rs61748396
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
|
24399845 |
2014 |
rs61749724
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
MECP2 duplication: possible cause of severe phenotype in females.
|
24458799 |
2014 |
rs61749724
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
|
24399845 |
2014 |
rs61750240
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
MECP2 duplication: possible cause of severe phenotype in females.
|
24458799 |
2014 |
rs61750240
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
|
24399845 |
2014 |
rs61750241
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
|
24399845 |
2014 |
rs61750241
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
MECP2 duplication: possible cause of severe phenotype in females.
|
24458799 |
2014 |
rs61751443
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
MECP2 duplication: possible cause of severe phenotype in females.
|
24458799 |
2014 |
rs61751443
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
|
24399845 |
2014 |
rs1557136758
|
|
CT |
0.700 |
CausalMutation |
CLINVAR |
Using a large international sample to investigate epilepsy in Rett syndrome.
|
23421866 |
2013 |