Variant: rs1554774973 

    present in Gene: NTRK2
    present in Chromosome: 9
    Position on Chromosome: 84955504
    Alleles of this Variant: C/T

rs1554774973 in NTRK2 gene and Obesity, Hyperphagia, and Developmental Delay PMID 27884935 2017 Diagnostic value of exome and whole genome sequencing in craniosynostosis.

PMID 29100083 2017 High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.

PMID 15494731 2004 A de novo mutation affecting human TrkB associated with severe obesity and developmental delay.