{{Rsnum
|rsid=2435207
|Gene=MAPT
|Chromosome=17
|position=45981562
|Orientation=plus
|GMAF=0.2833
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MAPT
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 7.1 | 56.6 | 36.3
| HCB | 3.6 | 34.3 | 62.0
| JPT | 5.3 | 41.6 | 53.1
| YRI | 5.4 | 41.5 | 53.1
| ASW | 3.5 | 38.6 | 57.9
| CHB | 3.6 | 34.3 | 62.0
| CHD | 6.4 | 30.3 | 63.3
| GIH | 4.0 | 28.7 | 67.3
| LWK | 11.9 | 50.5 | 37.6
| MEX | 13.8 | 34.5 | 51.7
| MKK | 7.7 | 38.5 | 53.8
| TSI | 4.9 | 33.3 | 61.8
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19558713
|Title=Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease
|OA=1
}}

{{PMID Auto
|PMID=15297935
|Title=Linkage disequilibrium and association of MAPT H1 in Parkinson disease.
|OA=1
}}

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

{{PMID Auto
|PMID=21898123
|Title=The age at motor symptoms onset in LRRK2-associated Parkinson's disease is affected by a variation in the MAPT locus: a possible interaction.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}