Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation 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: 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: 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: rs61750240
rs61750240
A 0.700 CausalMutation CLINVAR MECP2 duplication: possible cause of severe phenotype in females. 24458799

2014

dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation CLINVAR Using a large international sample to investigate epilepsy in Rett syndrome. 23421866

2013

dbSNP: rs61750240
rs61750240
A 0.700 CausalMutation CLINVAR Using a large international sample to investigate epilepsy in Rett syndrome. 23421866

2013

dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation CLINVAR Rett syndrome: revised diagnostic criteria and nomenclature. 21154482

2010

dbSNP: rs61750240
rs61750240
A 0.700 CausalMutation CLINVAR Rett syndrome: revised diagnostic criteria and nomenclature. 21154482

2010

dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation CLINVAR Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome. 18337588

2008

dbSNP: rs61750240
rs61750240
A 0.700 CausalMutation CLINVAR Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome. 18337588

2008

dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation CLINVAR MECP2 mutations in males. 17351020

2007

dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation CLINVAR Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2. 17267601

2007

dbSNP: rs61750240
rs61750240
A 0.700 CausalMutation CLINVAR Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2. 17267601

2007

dbSNP: rs61750240
rs61750240
A 0.700 CausalMutation CLINVAR MECP2 mutations in males. 17351020

2007

dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation CLINVAR Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH. 16169931

2006

dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation CLINVAR Early progressive encephalopathy in boys and MECP2 mutations. 16832102

2006

dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation CLINVAR Male Rett phenotypes in T158M and R294X MeCP2-mutations. 17236109

2006

dbSNP: rs61750240
rs61750240
A 0.700 CausalMutation CLINVAR Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH. 16169931

2006

dbSNP: rs61750240
rs61750240
A 0.700 CausalMutation CLINVAR Early progressive encephalopathy in boys and MECP2 mutations. 16832102

2006

dbSNP: rs61750240
rs61750240
A 0.700 CausalMutation CLINVAR Male Rett phenotypes in T158M and R294X MeCP2-mutations. 17236109

2006

dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation CLINVAR Macrocephalic mental retardation associated with a novel C-terminal MECP2 frameshift deletion. 15558314

2005

dbSNP: rs61750240
rs61750240
A 0.700 CausalMutation CLINVAR Macrocephalic mental retardation associated with a novel C-terminal MECP2 frameshift deletion. 15558314

2005

dbSNP: rs1557137745
rs1557137745
A 0.700 GeneticVariation CLINVAR Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome. 15057977

2004