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SNP information rs10886471

RS10886471

Normal allele: CC

The GRK5 variant is associated with the efficacy of repaglinide in patients with type 2 diabetes mellitus.

Polymorphism rs10886471 is related to topics like this:

Type 2 diabetes genetic

Type 2 diabetes is the most prevalent and impactful subtype of diabetes worldwide, affecting around...


Research and publications:

  22961080   A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans.

  24843659   Insights into the genetic basis of type 2 diabetes.

  24864266   Genetics of type 2 diabetes: insights into the pathogenesis and its clinical application.

  25774817   Genetics of type 2 diabetes-pitfalls and possibilities.

  26919830   Association between genetic variants and characteristic symptoms of type 2 diabetes: A matched case-control study.

  26964836   Recent progress in genetic and epigenetic research on type 2 diabetes.

  27053236   Evaluation of type 2 diabetes genetic risk variants in Chinese adults: findings from 93,000 individuals from the China Kadoorie Biobank.

  28821857   CDKAL1 rs7756992 is associated with diabetic retinopathy in a Chinese population with type 2 diabetes.

  29663513   A variant of GRK5 is associated with the therapeutic efficacy of repaglinide in Chinese Han patients with type 2 diabetes mellitus.

  29773828   Single Nucleotide Polymorphisms in the G-Protein Coupled Receptor Kinase 5 (GRK5) Gene are associated with Plasma LDL-Cholesterol Levels in Humans.

  30081999   [Distribution of the diabetes related gene variants among Chinese population born in early 1960s].

  30907055   Effects of variants of 50 genes on diabetes risk among the Chinese population born in the early 1960s.

  34502231   Common Genetic Aberrations Associated with Metabolic Interferences in Human Type-2 Diabetes and Acute Myeloid Leukemia: A Bioinformatics Approach.

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