{{Rsnum
|rsid=63750129
|Chromosome=17
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=MAPT
|position=45996612
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MAPT
}}{{omim
|desc=[[Pick's disease]]
|id=157140
|rsnum=63750129
|variant=0015
}}

{{ClinVar
|rsid=63750129
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=44073978
|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.44073978A>C
|CLNSRC=Neurodegenerative Brain Diseases Group; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=ADM_174; 157140.0015
|CLNSIG=5
|CLNCUI=C0236642; C0236642
|CLNDBN=Pick's disease; not provided
|Disease=Pick's disease; not provided
|CLNACC=RCV000015328.24; RCV000084515.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1505:C0236642:172700:282:13092008
}}

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