Disease: Nephrolithiasis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs180177161
rs180177161
Entrez Id: 189
Gene Symbol: AGXT
AGXT
CUI: C0392525
Disease:
Nephrolithiasis 		C 0.700 GeneticVariation CLINVAR Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. 28893421 2018