{{Rsnum
|rsid=63750512
|Chromosome=17
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MAPT
|position=46024010
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MAPT
}}{{omim
|desc=[[Pick's disease]]
|id=157140
|rsnum=63750512
|variant=0011
}}{{ClinVar
|rsid=63750512
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=44101376
|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; 2
|CLNHGVS=NC_000017.10:g.44101376G>A; NC_000017.10:g.44101376G>C
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000015324.24; RCV000084553.1
|CLNDBN=Pick's disease; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1505:C0236642:172700:282:13092008
|CLNSRC=OMIM Allelic Variant; Neurodegenerative Brain Diseases Group
|CLNSRCID=157140.0011; ADM_193
|Disease=Pick's disease; not provided
}}