rs180177227, AGXT

N. diseases: 3
Disease: Nephrolithiasis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Nephrolithiasis
CUI: C0392525
Disease: Nephrolithiasis
0.700 GeneticVariation CLINVAR Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. 28893421 2018