Variant: rs1554923218 

    present in Gene: TH
    present in Chromosome: 11
    Position on Chromosome: 2167458
    Alleles of this Variant: G/C

rs1554923218 in TH gene and Movement Disorders PMID 20823027 2011 Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency.

PMID 20430833 2010 Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis.

PMID 24696406 2014 What is new for monoamine neurotransmitter disorders?