Variant: rs1555690779 

    present in Gene: RAB11B
    present in Chromosome: 19
    Position on Chromosome: 8399886
    Alleles of this Variant: G/A

rs1555690779 in RAB11B gene and NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER PMID 29106825 2017 Recurrent De Novo Mutations Disturbing the GTP/GDP Binding Pocket of RAB11B Cause Intellectual Disability and a Distinctive Brain Phenotype.