rs1467967
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1467967(A;A) |
| Make rs1467967(A;G) |
| Make rs1467967(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 45908813 |
| Gene | MAPT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1467967 |
| dbSNP (classic) | rs1467967 |
| ClinGen | rs1467967 |
| ebi | rs1467967 |
| HLI | rs1467967 |
| Exac | rs1467967 |
| Gnomad | rs1467967 |
| Varsome | rs1467967 |
| LitVar | rs1467967 |
| Map | rs1467967 |
| PheGenI | rs1467967 |
| Biobank | rs1467967 |
| 1000 genomes | rs1467967 |
| hgdp | rs1467967 |
| ensembl | rs1467967 |
| geneview | rs1467967 |
| scholar | rs1467967 |
| rs1467967 | |
| pharmgkb | rs1467967 |
| gwascentral | rs1467967 |
| openSNP | rs1467967 |
| 23andMe | rs1467967 |
| SNPshot | rs1467967 |
| SNPdbe | rs1467967 |
| MSV3d | rs1467967 |
| GWAS Ctlg | rs1467967 |
| GMAF | 0.3829 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[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 18541914] Variation in MAPT is associated with cerebrospinal fluid tau levels in the presence of amyloid-beta deposition.
[PMID 28415654] The associations between the MAPT polymorphisms and Alzheimer's disease risk: a meta-analysis.
