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SNP information rs17319721

RS17319721

Normal allele: GG

Albuminuria gene variant, is associated with the rate of increase in albuminuria in diabetic patients.

Polymorphism rs17319721 is related to topics like this:

Adpkd kidney disease

The most prevalent type of PKD is Autosomal dominant polycystic kidney disease (ADPKD). This...


Research and publications:

  19430482   Multiple loci associated with indices of renal function and chronic kidney disease.

  20222955   A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level.

  20383145   Genetic loci influencing kidney function and chronic kidney disease.

  20383146   New loci associated with kidney function and chronic kidney disease.

  20686651   Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases.

  21355061   CUBN is a gene locus for albuminuria.

  21931561   Genetic association for renal traits among participants of African ancestry reveals new loci for renal function.

  21980298   Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD.

  22492995   Validated SNPs for eGFR and their associations with albuminuria.

  23028791   Multiple loci associated with renal function in African Americans.

  23586973   Investigation of known estimated glomerular filtration rate loci in patients with type 2 diabetes.

  25238615   A gene variant in CERS2 is associated with rate of increase in albuminuria in patients with diabetes from ONTARGET and TRANSCEND.

  26776194   KIDNEY DISEASE GENETICS AND THE IMPORTANCE OF DIVERSITY IN PRECISION MEDICINE.

  27779570   The influence of living donor SHROOM3 and ABCB1 genetic variants on renal function after kidney transplantation.

  29016630   Association between kidney function and genetic polymorphisms in atherosclerotic and chronic kidney diseases: A cross-sectional study in Japanese male workers.

  29476007   Characterization of Coding/Noncoding Variants for SHROOM3 in Patients with CKD.

  30341149   SHROOM3-FYN Interaction Regulates Nephrin Phosphorylation and Affects Albuminuria in Allografts.

  31534799   Novel Haplotype Indicator for End-Stage Renal Disease Progression among Saudi Patients.

  32265040   Loci associated with genomic damage levels in chronic kidney disease patients and controls.

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