Variant: rs1554121872 

    present in Gene: CAMK2A
    present in Chromosome: 5
    Position on Chromosome: 150250270
    Alleles of this Variant: T/G

rs1554121872 in CAMK2A gene and Delayed speech and language development PMID 29100089 2017 De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.

rs1554121872 in CAMK2A gene and Global developmental delay PMID 29100089 2017 De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.

rs1554121872 in CAMK2A gene and Gross motor development delay PMID 29100089 2017 De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.

rs1554121872 in CAMK2A gene and MENTAL RETARDATION, AUTOSOMAL DOMINANT 53 PMID 28130356 2017 A Novel Human CAMK2A Mutation Disrupts Dendritic Morphology and Synaptic Transmission, and Causes ASD-Related Behaviors.

PMID 29100089 2017 De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.

PMID 29560374 2018 De novo variants in CAMK2A and CAMK2B cause neurodevelopmental disorders.

PMID 25533962 2015 Large-scale discovery of novel genetic causes of developmental disorders.

rs1554121872 in CAMK2A gene and Movement Disorders PMID 29100089 2017 De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.

rs1554121872 in CAMK2A gene and Muscle hypotonia PMID 29100089 2017 De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.

rs1554121872 in CAMK2A gene and Poor school performance PMID 29100089 2017 De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.