Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7652589
rs7652589
CUI: C0022650
Disease: Kidney Calculi
Kidney Calculi
0.060 GeneticVariation BEFREE Epidemiological studies observed that calcium nephrolithiasis was associated with polymorphisms of the CaSR gene regulatory region, rs6776158, located within the promoter-1, rs1501899 located in the intron 1, and rs7652589 in the 5'-untranslated region. 30446806

2019

dbSNP: rs7652589
rs7652589
CUI: C0022650
Disease: Kidney Calculi
Kidney Calculi
0.060 GeneticVariation BEFREE Our study showed that CaSR rs7652589 polymorphism had a significant effect on the risk of developing calcium nephrolithiasis in the population of Yi nationality in Southwestern China. 29682741

2018

dbSNP: rs7652589
rs7652589
CUI: C0022650
Disease: Kidney Calculi
Kidney Calculi
0.060 GeneticVariation BEFREE CASR rs7652589_rs1801725 AG haplotype was 1.5-fold more frequent in nephrolithiasis-related ESRD than the GG haplotype (P = 0.004). 29763933

2018

dbSNP: rs7652589
rs7652589
CUI: C0022650
Disease: Kidney Calculi
Kidney Calculi
0.060 GeneticVariation BEFREE Associations of the calcium-sensing receptor gene CASR rs7652589 SNP with nephrolithiasis and secondary hyperparathyroidism in haemodialysis patients. 27739473

2016

dbSNP: rs7652589
rs7652589
CUI: C0022650
Disease: Kidney Calculi
Kidney Calculi
0.060 GeneticVariation BEFREE Arg990Gly is located on exon 7 and produces a gain of the CaSR function. rs7652589 and rs1501899 were also associated with nephrolithiasis in patients with normal citrate excretion. 22660550

2012

dbSNP: rs7652589
rs7652589
CUI: C0022650
Disease: Kidney Calculi
Kidney Calculi
0.060 GeneticVariation BEFREE Therefore, it is a candidate gene for calcium nephrolithiasis.In a case-control study we found an association between the normocitraturic stone formers and two SNPs of CaSR, located near the promoters region (rs7652589 and rs1501899). 22107799

2011