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SNP information rs199533

RS199533

Normal allele: GG

NSF replication carries a genetic risk underlying Parkinson's disease.

Polymorphism rs199533 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:

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

  20711177   Common genetic variations in the HLA region are associated with sporadic late-onset Parkinson's disease.

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

  21425343   Replication of MAPT and SNCA, but not PARK16-18, as Parkinson's disease susceptibility genes.

  21812969   Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.

  21876681   A genome-wide gene environment study identifies the glutamate receptor gene GRIN2A as a modifier gene for Parkinson's disease through interaction with coffee.

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

  25778476   A novel Alzheimer disease locus located near the gene encoding tau protein.

  27466229   Establishing DNA methylation levels in the brain indicates a risk factor for Parkinson's disease.

  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.

  29315334   Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies.

  30154825   To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes.

  32651314   Whole exome sequencing analysis of Alzheimer's disease in non-APOE*4 carriers.

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