Disease: Primary hyperoxaluria, type I ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs180177303
rs180177303
Entrez Id: 189
Gene Symbol: AGXT
AGXT
CUI: C0268164
Disease:
Primary hyperoxaluria, type I 		T 0.700 CausalMutation CLINVAR Primary hyperoxaluria type I: a model for multiple mutations in a monogenic disease within a distinct ethnic group. 10541294 1999