TDO2, tryptophan 2,3-dioxygenase, 6999

N. diseases: 89; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553957997
rs1553957997
Entrez Id: 6999
Gene Symbol: TDO2
TDO2
CUI: C2931837
Disease:
Familial hypertryptophanemia 		0.700 GeneticVariation UNIPROT Hypertryptophanemia due to tryptophan 2,3-dioxygenase deficiency. 28285122 2017