rs201331677, SLC34A1

N. diseases: 2
Disease: Nephrocalcinosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Nephrocalcinosis
CUI: C0027709
Disease: Nephrocalcinosis
0.700 GeneticVariation CLINVAR Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. 28893421 2018