Gene: TH ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554923218
rs1554923218
TH
C 0.700 CausalMutation CLINVAR What is new for monoamine neurotransmitter disorders? 24696406

2014
dbSNP: rs1554923218
rs1554923218
TH
C 0.700 CausalMutation CLINVAR Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency. 20823027

2011
dbSNP: rs1554923218
rs1554923218
TH
C 0.700 CausalMutation CLINVAR Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis. 20430833

2010