Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs180177241
rs180177241
AGXT
A 0.700 GeneticVariation CLINVAR Performance evaluation of Sanger sequencing for the diagnosis of primary hyperoxaluria and comparison with targeted next generation sequencing. 25629080

2015
dbSNP: rs180177241
rs180177241
AGXT
AC 0.700 CausalMutation CLINVAR Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene. 19479957

2009
dbSNP: rs180177241
rs180177241
AGXT
A 0.700 CausalMutation CLINVAR