Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1372180906
rs1372180906
TH ; MIR4686
T 0.700 CausalMutation CLINVAR Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype. 21465550

2011
dbSNP: rs1372180906
rs1372180906
TH ; MIR4686
T 0.700 CausalMutation CLINVAR Mutations in the cyclic adenosine monophosphate response element of the tyrosine hydroxylase gene. 17696123

2007