rs3785883

Orientation

plus

Stabilized

plus

Make rs3785883(A;A)

Make rs3785883(A;G)

Make rs3785883(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

45977067

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs3785883
dbSNP (classic)	rs3785883
ClinGen	rs3785883
ebi	rs3785883
HLI	rs3785883
Exac	rs3785883
Gnomad	rs3785883
Varsome	rs3785883
LitVar	rs3785883
Map	rs3785883
PheGenI	rs3785883
Biobank	rs3785883
1000 genomes	rs3785883
hgdp	rs3785883
ensembl	rs3785883
geneview	rs3785883
scholar	rs3785883
google	rs3785883
pharmgkb	rs3785883
gwascentral	rs3785883
openSNP	rs3785883
23andMe	rs3785883
SNPshot	rs3785883
SNPdbe	rs3785883
MSV3d	rs3785883
GWAS Ctlg	rs3785883

GMAF

0.1708

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 19558713] Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease

[PMID 15297935] 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 17266761] Haplotype-based association analysis of the MAPT locus in late onset Alzheimer's disease.

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

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

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

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

[PMID 19063963] Genetic susceptibility in Parkinson's disease.

[PMID 28415654] The associations between the MAPT polymorphisms and Alzheimer's disease risk: a meta-analysis.