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SNP information rs725613

RS725613

Normal allele: TT

Variation in the CLEC16A gene shows a consistent disease association with both multiple sclerosis and type 1 diabetes.

Polymorphism rs725613 is related to topics like this:

Type 1 diabetes is it genetic

Our latest inclusion in the health report is the Type 1 Diabetes Genetic Risk Score, aimed at...

Research and publications:

  17632545   A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.

  18840781   Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.

  18946483   Variation within the CLEC16A gene shows consistent disease association with both multiple sclerosis and type 1 diabetes in Sardinia.

  19178520   Intron polymorphism in the KIAA0350 gene is reproducibly associated with susceptibility to type 1 diabetes (T1D) in the Han Chinese population.

  20405052   The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.

  20849399   More CLEC16A gene variants associated with multiple sclerosis.

  21309755   Genetic mapping of vascular calcified plaque loci on chromosome 16p in European Americans from the diabetes heart study.

  21826374   Selective IgA deficiency in autoimmune diseases.

  21989056   Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene.

  22257840   Association of primary biliary cirrhosis with variants in the CLEC16A, SOCS1, SPIB and SIAE immunomodulatory genes.

  22778732   The Correlation between the CLEC16A Gene and Genetic Susceptibility to Type 1 Diabetes in Chinese Children.

  23133532   Polymorphisms in the inflammatory genes CIITA, CLEC16A and IFNG influence BMD, bone loss and fracture in elderly women.

  25690649   Multiple genetic variants associated with primary biliary cirrhosis in a Han Chinese population.

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