Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1557136758
rs1557136758
CT 0.700 CausalMutation CLINVAR Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study. 27354166

2016

dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation CLINVAR Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study. 27354166

2016

dbSNP: rs28934906
rs28934906
A 0.700 CausalMutation CLINVAR Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study. 27354166

2016

dbSNP: rs61748396
rs61748396
C 0.700 CausalMutation CLINVAR Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study. 27354166

2016

dbSNP: rs61749724
rs61749724
C 0.700 CausalMutation CLINVAR Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study. 27354166

2016

dbSNP: rs61750240
rs61750240
A 0.700 CausalMutation CLINVAR Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study. 27354166

2016

dbSNP: rs61750241
rs61750241
G 0.700 CausalMutation CLINVAR Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study. 27354166

2016

dbSNP: rs61751443
rs61751443
G 0.700 GeneticVariation CLINVAR Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study. 27354166

2016

dbSNP: rs1557136758
rs1557136758
CT 0.700 CausalMutation CLINVAR Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. 24399845

2014

dbSNP: rs1557136758
rs1557136758
CT 0.700 CausalMutation CLINVAR MECP2 duplication: possible cause of severe phenotype in females. 24458799

2014

dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation CLINVAR Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. 24399845

2014

dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation CLINVAR MECP2 duplication: possible cause of severe phenotype in females. 24458799

2014

dbSNP: rs28934906
rs28934906
A 0.700 CausalMutation CLINVAR MECP2 duplication: possible cause of severe phenotype in females. 24458799

2014

dbSNP: rs28934906
rs28934906
A 0.700 CausalMutation CLINVAR Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. 24399845

2014

dbSNP: rs61748396
rs61748396
C 0.700 CausalMutation CLINVAR Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. 24399845

2014

dbSNP: rs61748396
rs61748396
C 0.700 CausalMutation CLINVAR MECP2 duplication: possible cause of severe phenotype in females. 24458799

2014

dbSNP: rs61749724
rs61749724
C 0.700 CausalMutation CLINVAR MECP2 duplication: possible cause of severe phenotype in females. 24458799

2014

dbSNP: rs61749724
rs61749724
C 0.700 CausalMutation CLINVAR Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. 24399845

2014

dbSNP: rs61750240
rs61750240
A 0.700 CausalMutation CLINVAR MECP2 duplication: possible cause of severe phenotype in females. 24458799

2014

dbSNP: rs61750240
rs61750240
A 0.700 CausalMutation CLINVAR Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. 24399845

2014

dbSNP: rs61750241
rs61750241
G 0.700 CausalMutation CLINVAR MECP2 duplication: possible cause of severe phenotype in females. 24458799

2014

dbSNP: rs61750241
rs61750241
G 0.700 CausalMutation CLINVAR Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. 24399845

2014

dbSNP: rs61751443
rs61751443
G 0.700 GeneticVariation CLINVAR Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. 24399845

2014

dbSNP: rs61751443
rs61751443
G 0.700 GeneticVariation CLINVAR MECP2 duplication: possible cause of severe phenotype in females. 24458799

2014

dbSNP: rs1557136758
rs1557136758
CT 0.700 CausalMutation CLINVAR Using a large international sample to investigate epilepsy in Rett syndrome. 23421866

2013