{{Rsnum
|rsid=242559
|Gene=MAPT
|Chromosome=17
|position=45948522
|Orientation=plus
|GMAF=0.2479
|Gene_s=MAPT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 57.5 | 41.6 | 0.9
| HCB | 93.3 | 6.7 | 0.0
| JPT | 83.2 | 15.9 | 0.9
| YRI | 17.0 | 51.0 | 32.0
| ASW | 26.3 | 52.6 | 21.1
| CHB | 93.3 | 6.7 | 0.0
| CHD | 89.9 | 10.1 | 0.0
| GIH | 82.0 | 17.0 | 1.0
| LWK | 38.2 | 48.2 | 13.6
| MEX | 56.9 | 32.8 | 10.3
| MKK | 29.0 | 49.0 | 21.9
| TSI | 40.2 | 45.1 | 14.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=22451204
|Title=Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2
|OA=1
}}

{{PMID Auto
|PMID=18072964
|Title=No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease.
|OA=1
}}

{{PMID Auto
|PMID=18509094
|Title=Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}