rs2471738
| Orientation | plus |
| Stabilized | plus |
| Make rs2471738(C;C) |
| Make rs2471738(C;T) |
| Make rs2471738(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 45998697 |
| Gene | MAPT, STH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2471738 |
| dbSNP (classic) | rs2471738 |
| ClinGen | rs2471738 |
| ebi | rs2471738 |
| HLI | rs2471738 |
| Exac | rs2471738 |
| Gnomad | rs2471738 |
| Varsome | rs2471738 |
| LitVar | rs2471738 |
| Map | rs2471738 |
| PheGenI | rs2471738 |
| Biobank | rs2471738 |
| 1000 genomes | rs2471738 |
| hgdp | rs2471738 |
| ensembl | rs2471738 |
| geneview | rs2471738 |
| scholar | rs2471738 |
| rs2471738 | |
| pharmgkb | rs2471738 |
| gwascentral | rs2471738 |
| openSNP | rs2471738 |
| 23andMe | rs2471738 |
| SNPshot | rs2471738 |
| SNPdbe | rs2471738 |
| MSV3d | rs2471738 |
| GWAS Ctlg | rs2471738 |
| GMAF | 0.2002 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19684401] Genetic Interaction between Tau and the Apolipoprotein E Receptor LRP1 Increases Alzheimer's Disease Risk
[PMID 20951764] High cerebrospinal tau levels are associated with the rs242557 tau gene variant and low cerebrospinal ?-amyloid in Parkinson disease
[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 18541914] Variation in MAPT is associated with cerebrospinal fluid tau levels in the presence of amyloid-beta deposition.
[PMID 18813964] Alzheimer's disease risk variants show association with cerebrospinal fluid amyloid beta.
[PMID 18830724] Assessment of Alzheimer's disease case-control associations using family-based methods.
[PMID 19558713] Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease.
[PMID 20574532] Intermediate phenotypes identify divergent pathways to Alzheimer's disease.
[PMID 28415654] The associations between the MAPT polymorphisms and Alzheimer's disease risk: a meta-analysis.
