Normal allele: GG
Polymorphism rs3785883 is related to topics like this:
Research and publications:
15297935 Linkage disequilibrium and association of MAPT H1 in Parkinson 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.
18509094 Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study.
19063963 Genetic predisposition to Parkinson'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.
31234228 Association of MAPT H1 subhaplotypes with neuropathology of lewy body disease.