{{Rsnum
|rsid=1052553
|Gene=MAPT
|Chromosome=17
|position=45996523
|Orientation=plus
|GMAF=0.1175
|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 | 59.3 | 39.8 | 0.9
| HCB | 100.0 | 0.0 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 98.0 | 2.0 | 0.0
| ASW | 80.7 | 17.5 | 1.8
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 82.2 | 16.8 | 1.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 70.7 | 22.4 | 6.9
| MKK | 87.8 | 9.0 | 3.2
| TSI | 42.2 | 44.1 | 13.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=19912324
|Title=Association of the MAPT locus with Parkinson's disease
|OA=1
}}

{{PMID Auto
|PMID=21159074
|Title=SNCA, MAPT, and GSK3B in Parkinson disease: a gene-gene interaction study
}}

{{ClinVar
|rsid=1052553
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=44073889
|CHROM=17
|GMAF=0.1177
|dbSNPBuildID=86
|SSR=0
|SAO=0
|VP=0x05016800000015051f100100
|GENEINFO=MAPT:4137
|GENE_NAME=MAPT
|GENE_ID=4137
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.44073889A>G
|CLNSIG=1
|Tags=PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD
|CAF=0.8825; 0.1175
|COMMON=1
|CLNACC=RCV000084512.1
|CLNDBN=not provided
|CLNSRC=Neurodegenerative Brain Diseases Group
|CLNSRCID=ADM_219
|Disease=not provided
}}

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

{{PMID|20116045|OA=1
}} The distribution and most recent common ancestor of the 17q21 inversion in humans.

{{PMID|21391235|OA=1
}} Independent and joint effects of the MAPT and SNCA genes in Parkinson disease.

{{PMID Auto
|PMID=23911736
|Title=MAPT Gene Rs1052553 Variant is not Associated with the Risk for Multiple Sclerosis
}}

{{PMID Auto
|PMID=23962496
|Title=The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants
}}

{{PMID Auto
|PMID=24372973
|Title=The microtubule associated protein tau H1 haplotype and risk of essential tremor
}}

{{PMID Auto
|PMID=23001634
|Title=MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome.
}}

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