{{Rsnum
|rsid = 12938245
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Gene = MAPT
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=17
|position=45983243
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MAPT
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=12938245
|allele=T
|frequency=0
|uid=1103645332553
|type=heterozygous_SNP
|hugo=MAPT
|ensembl gene=ENSG00000186868
|ensembl transcript=ENST00000262410
|sift=TOLERATED
|disease=Defects in MAPT may be a cause of hereditary dysphasic disinhibition dementia (HDDD) (MIM:607485). HDDD is a frontotemporal dementia characterized by progressive cognitive deficits with memory loss and personality changes, severe dysphasic disturbances leading to mutism, and hyperphagia.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}