Variant: rs761399728 

    present in Gene: GNB5
    present in Chromosome: 15
    Position on Chromosome: 52153947
    Alleles of this Variant: G/A

rs761399728 in GNB5 gene and LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA PMID 27523599 2016 GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability.

PMID 27677260 2016 GNB5 mutation causes a novel neuropsychiatric disorder featuring attention deficit hyperactivity disorder, severely impaired language development and normal cognition.