Variant: rs869312821 

    present in Gene: GNB1
    present in Chromosome: 1
    Position on Chromosome: 1806515
    Alleles of this Variant: T/C

rs869312821 in GNB1 gene and Global developmental delay PMID 27108799 2016 Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures.

rs869312821 in GNB1 gene and Infantile muscular hypotonia PMID 27108799 2016 Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures.

rs869312821 in GNB1 gene and Muscle hypotonia PMID 27108799 2016 Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures.

rs869312821 in GNB1 gene and Poor school performance PMID 27108799 2016 Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures.