TH, tyrosine hydroxylase, 7054

N. diseases: 321; N. variants: 71
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10770141
rs10770141
Entrez Id: 7054;100616126
Gene Symbol: TH;MIR4686
TH;MIR4686
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE The proximal promoter block contained four common variants, and its haplotypes and SNPs (especially C-824T, rs10770141) predicted catecholamine secretion, environmental stress-induced BP increments, and hypertension. 20571875 2010
dbSNP: rs1213545562
rs1213545562
Entrez Id: 7054
Gene Symbol: TH
TH
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE To investigate the biochemical and genetic background of this disease we investigated the genotypes for two polymorphisms associated with hypertension: TH01, a tetrameric microsatellite in the tyrosine hydroxylase gene and the single nucleotide polymorphism C825T in the GNB3 gene in 116 sudden deaths from MI (78 males, 38 females) and in a control group of 137 deaths from natural causes other than MI (52 males, 85 females). 16139102 2005
dbSNP: rs1384915680
rs1384915680
Entrez Id: 7054
Gene Symbol: TH
TH
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE To investigate the biochemical and genetic background of this disease we investigated the genotypes for two polymorphisms associated with hypertension: TH01, a tetrameric microsatellite in the tyrosine hydroxylase gene and the single nucleotide polymorphism C825T in the GNB3 gene in 116 sudden deaths from MI (78 males, 38 females) and in a control group of 137 deaths from natural causes other than MI (52 males, 85 females). 16139102 2005