IDO1, indoleamine 2,3-dioxygenase 1, 3620

N. diseases: 295; N. variants: 7
Disease: Huntington Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9657182
rs9657182
Entrez Id: 3620
Gene Symbol: IDO1
IDO1
CUI: C0020179
Disease:
Huntington Disease 		0.010 GeneticVariation BEFREE The rs9657182 TT genotype associates with infection-related mortality of HD patients. 29935858 2018