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SNP information rs393152

RS393152

Normal allele: GG

Genetic risk underlying Parkinson's disease.

Polymorphism rs393152 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:

  18985386   Genomewide association study for susceptibility genes contributing to familial Parkinson disease.

  19915575   Genome-wide association study identifies genetic risk underlying Parkinson's disease.

  20070850   Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.

  21248740   Genome-wide association study confirms extant PD risk loci among the Dutch.

  21412835   Common variants in the PARK and related genes loci and Parkinson's disease.

  21898123   Age of onset of motor symptoms in LRRK2-associated Parkinson's disease is influenced by variations in the MAPT locus: a possible interaction.

  22086882   No association between Parkinson disease alleles and the risk of melanoma.

  22551073   LDGIdb: a database of gene interactions inferred from long-range strong linkage disequilibrium between pairs of SNPs.

  23071545   Evaluation of Parkinson disease risk variants as expression-QTLs.

  24868370   Human genetic variation and Parkinson's disease.

  24931982   GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database.

  25687773   Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus.

  27494614   Big data predictive analytics: Parkinson's disease research using large, complex, heterogeneous, inconsistent, multi-source, and incomplete observations.

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

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