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SNP information rs6812193

RS6812193

Normal allele: CC

SCARB2 gene expression as an essential genetic component for Parkinson's disease.

Polymorphism rs6812193 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.

  21738488   A two-stage meta-analysis identified several new loci for Parkinson's disease.

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

  22465138   Study of the association of rs6812193 SCARB2 polymorphism with Parkinson's disease in Han Chinese.

  22531747   Study of the association between two novel single nucleotide polymorphisms and sporadic Parkinson's disease in the Chinese Han population.

  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.

  23419877   Is Parkinson disease associated with lysosomal integral membrane protein type-2?: challenges in interpreting association data.

  23473716   Study of the association of rs6812193 polymorphism with Parkinson's disease in the Greek population.

  24973356   Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies.

  25528405   Multi-locus analysis from genome-wide association studies in Parkinson's disease in mainland China.

  25820215   Association between rs6812193 polymorphism and sporadic susceptibility to Parkinson's disease.

  25929833   Genetic loci of Parkinson's disease in rapid eye movement sleep behavior disorder.

  26224037   No association of FAM47E rs6812193, SCARB2 rs6825004 and STX1B rs4889603 polymorphisms with Parkinson's disease was detected in the Chinese Han population.

  26793951   Integrative analyses of proteomics and RNA transcriptomics implicate mitochondrial processes, protein folding pathways and GWAS loci in Parkinson disease.

  27461410   Enrichment of risk SNPs in regulatory regions implicates diverse tissues in the etiology of Parkinson's disease.

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

  29664058   Relationships between Rapid Eye Movement Sleep Behavior Disorder and Neurodegenerative Diseases: Clinical Assessments, Biomarkers, and Treatment.

  30665447   Dementia with Lewy bodies: an update and outlook.

  33147747   Pathogenic Single Nucleotide Polymorphisms on Autophagy-Related Genes.

  33227372   Genetic variants and expression of the SCARB2 gene in the pathogenesis of Parkinson's disease in Russia.

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