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SNP information rs12456492

RS12456492

Normal allele: AA

The RIT2 rs12456492 polymorphism is associated with Parkinson's disease.

Polymorphism rs12456492 is related to topics like this:

Parkinson is a genetic disease

A disorder that progresses gradually within the nervous system is known as Parkinson's disease. It...


Research and publications:

  23635658   The RIT2 variant is not associated with Parkinson's disease in the Taiwanese population.

  25457028   RIT2 polymorphism is associated with Parkinson's disease in the Han population.

  25534083   RIT2 and STX1B polymorphisms are associated with Parkinson's disease.

  25559334   Assessing the association of RIT2 rs12456492 with Parkinson's disease in mainland China.

  26188085   RIT2 rs12456492 polymorphism and risk of Parkinson's disease: a meta-analysis.

  26334395   Genetic association of RIT2 rs12456492 polymorphism and Parkinson's disease susceptibility in Asian populations: a meta-analysis.

  27456991   Genetic associations of the thyroid stimulating hormone receptor gene with Graves diseases and Graves ophthalmopathy: A meta-analysis.

  27504496   Trans-pQTL study identifies immune crosstalk between Parkinson and Alzheimer loci.

  27889863   Investigating the genetic association between RIT2 and Parkinson's disease in a Han population.

  28927418   A systematic review and integrative approach to decipher the overall molecular link between levodopa response and Parkinson's disease.

  31818509   Association of RIT2 and RAB7L1 with Parkinson's disease: a case-control study in a Taiwanese cohort and meta-analysis in Asian populations.

  33987465   Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes.

  34305570   pH-eQTL interaction at the Parkinson's disease risk locus RIT2-SYT4 in the substantia nigra.

  35695987   Neurodegeneration-related gene polymorphisms are associated with Parkinson's disease risk.

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