Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs759330
rs759330
BGLAP ; PAQR6 ; PMF1-BGLAP
CUI: C1833683
Disease: NEPHROLITHIASIS, CALCIUM OXALATE
NEPHROLITHIASIS, CALCIUM OXALATE 		A 0.700 GeneticVariation CLINVAR A whole genome SNP genotyping by DNA microarray and candidate gene association study for kidney stone disease. 24886237

2014