rs1553957997, TDO2

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Familial hypertryptophanemia
CUI: C2931837
Disease: Familial hypertryptophanemia
0.700 GeneticVariation UNIPROT Hypertryptophanemia due to tryptophan 2,3-dioxygenase deficiency. 28285122 2017