Variant: rs1057521721 

    present in Gene: GRIA3
    present in Chromosome: X
    Position on Chromosome: 123428020
    Alleles of this Variant: G/A

rs1057521721 in GRIA3 gene and Gross motor development delay PMID 29016847 2017 A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability.

rs1057521721 in GRIA3 gene and Profound global developmental delay PMID 29016847 2017 A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability.

rs1057521721 in GRIA3 gene and Severe intellectual disability PMID 29016847 2017 A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability.

rs1057521721 in GRIA3 gene and Sleep disturbances PMID 29016847 2017 A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability.