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rs3785883

From SNPedia

Orientationplus
Stabilizedplus
Make rs3785883(A;A)
Make rs3785883(A;G)
Make rs3785883(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position45977067
GeneMAPT
is asnp
is mentioned by
dbSNPrs3785883
ebirs3785883
HLIrs3785883
Exacrs3785883
Varsomers3785883
Maprs3785883
PheGenIrs3785883
hapmaprs3785883
1000 genomesrs3785883
hgdprs3785883
ensemblrs3785883
gopubmedrs3785883
geneviewrs3785883
scholarrs3785883
googlers3785883
pharmgkbrs3785883
gwascentralrs3785883
openSNPrs3785883
23andMers3785883
23andMe allrs3785883
SNP Nexus

SNPshotrs3785883
SNPdbers3785883
MSV3drs3785883
GWAS Ctlgrs3785883
GMAF0.1708
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19558713OA-icon.png] Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease

[PMID 15297935OA-icon.png] Linkage disequilibrium and association of MAPT H1 in Parkinson disease.

[PMID 17192721] Association of tau haplotype-tagging polymorphisms with Parkinson's disease in diverse ethnic Parkinson's disease cohorts.

[PMID 17266761OA-icon.png] Haplotype-based association analysis of the MAPT locus in late onset Alzheimer's disease.

[PMID 18065436OA-icon.png] The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family.

[PMID 18072964OA-icon.png] No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease.

[PMID 18509094OA-icon.png] Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study.

[PMID 18541914OA-icon.png] Variation in MAPT is associated with cerebrospinal fluid tau levels in the presence of amyloid-beta deposition.

[PMID 19063963OA-icon.png] Genetic susceptibility in Parkinson's disease.