{{Rsnum
|rsid=63750425
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MAPT
|position=46018675
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MAPT
}}{{omim
|id=157140
|rsnum=63750425
|variant=0023
}}

{{ClinVar
|rsid=63750425
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=44096041
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=MAPT:4137
|GENE_NAME=MAPT
|GENE_ID=4137
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.44096041C>T
|CLNSRC=Neurodegenerative Brain Diseases Group; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=ADM_191; 157140.0023
|CLNSIG=5
|CLNCUI=C0038868; C0038868
|CLNDBN=Progressive supranuclear ophthalmoplegia; not provided
|Disease=Progressive supranuclear ophthalmoplegia; not provided
|CLNACC=RCV000015337.24; RCV000084550.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1505:C0038868:601104:240071:28978003
}}

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