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SNP information rs3785883

RS3785883

Normal allele: GG

Polymorphism rs3785883 is related to topics like this:

Alzheimer's disease is hereditary

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


Research and publications:

  15297935   Linkage disequilibrium and association of MAPT H1 in Parkinson disease.

  17192721   Association of tau haplotype-marking polymorphisms with Parkinson's disease in different ethnic cohorts with Parkinson's disease.

  17266761   Haplotype-based association analysis of the MAPT locus in late-onset Alzheimer's disease.

  18065436   The tauopathy associated with mutation 3 in intron 10 of Tau: characterization of the MSTD family.

  18072964   No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease.

  18509094   Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study.

  18541914   Variation in MAPT is associated with cerebrospinal fluid tau levels in the presence of amyloid-beta deposition.

  19063963   Genetic predisposition to Parkinson's disease.

  19558713   The role of the H1 haplotype of the microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease.

  20862329   SNPs associated with cerebrospinal fluid phospho-tau levels influence the rate of decline in Alzheimer's disease.

  21397051   Variation in MAPT is not a contributing factor to the incomplete penetrance in LHON.

  24851016   Genetic studies in human prion diseases.

  27147968   Genetic Architecture of MAPT Gene Region in Parkinson Disease Subtypes.

  27900365   Genome sequencing in a case of Niemann-Pick type C.

  28402959   Meta-analysis of the association between variants in MAPT and neurodegenerative diseases.

  28415654   Association between MAPT polymorphisms and risk of Alzheimer's disease: a meta-analysis.

  29098924   Association of microtubule-associated protein tau gene polymorphisms with risk of sporadic Alzheimer's disease: a meta-analysis.

  30329219   Association of polymorphisms marking MAPT haplotypes with cerebrospinal fluid biomarkers of Alzheimer's disease: a pilot study in a Croatian cohort.

  31234228   Association of MAPT H1 subhaplotypes with neuropathology of lewy body disease.

Is OCD obsessive compulsive disorder genetic

Obsessive-compulsive disorder (OCD) is a mental health condition characterized by features known as...

Suicide genetic

Suicide is a serious public health crisis and it has been getting progressively worse. In the past...

Genetics and atherosclerosis

Atherosclerosis is a progressive inflammatory disorder that underlies coronary artery disease (CAD)...

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