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SNP information rs2102808

RS2102808

Normal allele: GG

Increased risk of Parkinson's disease at a young age.

Polymorphism rs2102808 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:

  21738487   Genome-wide internet-based association study identifies two new loci and a significant genetic component of Parkinson's disease.

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

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

  22210626   Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.

  22892372   Using genome-wide integrated trait analysis to quantify “missing heritability” in Parkinson's disease.

  22911860   Genome-wide assessment of Parkinson's disease in young people from Finland.

  24631562   Association analysis of STK39, MCCC1/LAMP3 and sporadic PD in the Chinese Han population.

  26090850   Exon resequencing of the Parkinson's disease locus of chromosome 2q24.3.

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

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Dementia is genetic

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Alzheimer's disease is hereditary

Alzheimer's disease is a degenerative brain disease that causes dementia, resulting in a gradual...

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